Method of recovering lactide
10336882 ยท 2019-07-02
Assignee
Inventors
Cpc classification
Y02W30/62
GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
C08J2367/04
CHEMISTRY; METALLURGY
B29B7/845
PERFORMING OPERATIONS; TRANSPORTING
B29C48/763
PERFORMING OPERATIONS; TRANSPORTING
B29B17/00
PERFORMING OPERATIONS; TRANSPORTING
B29K2067/00
PERFORMING OPERATIONS; TRANSPORTING
B29C48/40
PERFORMING OPERATIONS; TRANSPORTING
International classification
Abstract
A method of recovering lactide which includes introducing a molten resin composition that contains a polylactic acid, a depolymerization catalyst and a carrier resin into a vent chamber (3) that is maintained under a reduced pressure using a first screw conveyer passage (11) that extends in the vent chamber (3), gasifying the lactide contained in the molten resin composition, and recovering a gaseous lactide from the vent chamber, wherein a second screw conveyer passage (60) is provided under the first screw conveyer passage (11) in the vent chamber (3) to recover the carrier resin.
Claims
1. A method of recovering lactide comprising introducing a molten resin composition that contains a polylactic acid, a depolymerization catalyst and a carrier resin into a vent chamber that is maintained under a reduced pressure by using a first screw conveyer passage that is extending in the vent chamber, gasifying the lactide contained in said molten resin composition, and recovering a gaseous lactide from said vent chamber, wherein a second screw conveyer passage is provided under said first screw conveyer passage in said vent chamber to recover the carrier resin.
2. The method according to claim 1, wherein a return member is provided over said first screw conveyer passage to return resin masses formed accompanying the gasification of the lactide back to said first screw conveyer passage.
3. The method according to claim 1, wherein second conveyer screws extending in said second screw conveyer passage have a diameter SD2 that is set to be smaller than a diameter SD1 of first conveyer screws that are extending in said first screw conveyer passage.
4. The method according to claim 1, wherein a trapping apparatus is linked to said vent chamber to trap said gaseous lactide.
5. The method according to claim 1, wherein an upper wall of said vent chamber is provided with a vessel for receiving a refluxing liquid that falls down along said upper wall, said vessel being partitioned from said first screw conveyer passage.
6. The method according to claim 5, wherein the upper wall of said vent chamber is provided with a tilted peep window.
7. The method according to claim 1, wherein said second screw conveyer passage is communicated with an extruder for discharging the carrier resin.
8. The method according to claim 2, wherein said return member is a fall-down screw provided being engaged with the conveyer screws that are extending in said first screw conveyer passage.
9. A method of recovering lactide comprising introducing a molten resin composition that contains a polylactic acid, a depolymerization catalyst and a carrier resin into a vent chamber that is maintained under a reduced pressure by using a screw conveyer passage that is extending in the vent chamber, gasifying the lactide contained in said molten resin composition, and recovering a gaseous lactide from said vent chamber, wherein a return member is provided over the screw conveyer passage to return the resin masses formed accompanying the gasification of said lactide back to said screw conveyer passage.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
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MODES FOR CARRYING OUT THE INVENTION
(8) Referring to
(9) The present invention uses the above-mentioned recovering apparatus. Namely, a polylactic acid, a depolymerization catalyst and a carrier resin are thrown into a hopper of the extruder 1, and are melt-kneaded in a cylinder of the extruder 1 where the polylactic acid is depolymerized. The melt-kneaded product is then fed into the vent chamber 3 where a lactide formed by the depolymerization of the polylactic acid is gasified. The gasified lactide is then introduced into the trapping apparatus 5 that is communicated with the vent chamber 3, is liquefied through a gas-liquid separation tower 51 and a first condenser 53, and is recovered through a receiver 59. The carrier resin, on the other hand, is discharged from the carrier resin recovering chamber 4 under the vent chamber 3 through the extruder 6 for discharging the carrier resin.
(10) As the polylactic acid from which the lactide is to be recovered, there can be used those recovered from the market (post-consumer wastes), industrial wastes discharged from the resin processing manufacturers and out-of-specification resins generated in the step of producing polylactic acid resins. There can be, further, used those of the stereo-complex type in which L-lactic acid (PLLA) and D-lactic acid (PDLA) are mixed together, or those of the meso type in which L-lactic acid unit and D-lactic acid unit are present in a mixed manner in the molecular chains. Use of a virgin polylactic acid poses no problem, as a matter of course.
(11) Moreover, the polylactic acid that is used may include small amounts of copolymer units, e.g., may include units due to lactones, cyclic ethers, cyclic amides, alcohols or carboxylic acids, that are capable of copolymerizing with the lactide under the condition that not less than 50 mol % thereof are the lactic acid units.
(12) MgO is a representative example of the catalyst for depolymerizing the polylactic acid, and is most preferably used. However, there can also be used such alkaline earth metal oxides as CaO, SrO, BaO and the like. There can be, further, preferably used Tin(II)2-ethylhexanoate which is used as the polymerization catalyst and aluminum hydroxide (Al(OH).sub.3) which is a flame retarder. It is also allowable to use these catalysts as a mixture thereof. The depolymerization catalyst works to lower the temperature for depolymerizing the polylactic acid. Upon using the depolymerization catalyst, thermal decomposition of the polylactic acid is accelerated, and the polylactic acid acquires decreased molecular weights. For instance, the polylactic acid that possessed a molecular weight of about 200,000 when it was thrown into the hopper of the extruder 1 can be decomposed into a lactide of a molecular weight of 144. Further, MgO and the like are effective in suppressing the racemization phenomenon during the thermal reaction.
(13) The catalyst for depolymerizing the polylactic acid is used, usually, in an amount of 0.1 to 5 parts by mass per 100 parts by mass of the polylactic acid.
(14) The carrier resin is used for conveying a melt of the polylactic acid by screw and also works as a sealing material. As the carrier resin, there can be used various thermoplastic resins so far as they do not adversely affect the depolymerization of the polylactic acid and do not show reactivity to the lactide that is formed by the depolymerization of the polylactic acid. Usually, there can be used olefin resins such as polyethylene and polypropylene; polyester resins such as polyethylene terephthalate (PET) and the like; polyethers such as polycarbonate (PC) and the like; and styrol resins such as polystyrene (PS) and the like. Specifically preferably, there can be used HDPE, LDPE and PP having high melt viscosities.
(15) That is, the polylactic acids containing the lactide, in general, have melt viscosities that are considerably lower than those of the ordinary polymers though dependent upon their molecular weights. Therefore, the melt of the polylactic acid cannot be efficiently conveyed by the screw. This is because the screw turns almost empty-loaded. Accordingly, the carrier resin is used in combination to increase the viscosity of the molten resin that contains the melt of the polylactic acid in the extruder. The melt of the polylactic acid can then be efficiently conveyed by screws.
(16) Besides, the carrier resin has a melt viscosity higher than that of the polylactic acid that contains the lactide. By adding the carrier resin in certain amounts to the polylactic acid, and mixing and melting the two together, therefore, the gaps between the inner surface of the cylinder of the extruder and the screws are filled with the molten mixture which, therefore, can be conveyed by screws. Namely, the carrier resin enables the gaps between the inner surface of the cylinder and the screws to be sealed at all times, and the pressure in the vent chamber 3 can be effectively reduced.
(17) It is also allowable to use a carrier resin having a low melt viscosity. That is, the resin (PET, PC, PS or the like) does not by itself undergo the thermal decomposition if it has a thermal decomposition temperature higher than the depolymerization temperature of the PLA, and can be used to convey (move forward) the polylactic acid and the depolymerized product thereof by screws.
(18) In the present invention, the amount of the carrier resin is, usually, set to lie in a suitable range depending on the specifications of the apparatus. For instance, the amount thereof is set to be about 20 to about 10,000 parts by mass and, more preferably, 20 to 100 parts by mass per 100 parts by mass of the polylactic acid from the standpoint of attaining conveyance by screws and vacuum sealing. This amount is considerably smaller than the amounts that are usually employed. The reasons will be described later.
(19) The above-mentioned polylactic acid, depolymerization catalyst and carrier resin are thrown in predetermined amounts into the hopper of the extruder 1, and are melted and mixed together in the cylinder of the extruder 1.
(20) The interior of the cylinder is heated by a heater that is so provided as to cover the cylinder of the extruder 1. The components are melted and mixed together while being stirred and conveyed by the screws that are running in the cylinder, and the polylactic acid is depolymerized at a temperature of not lower than 250 C. As the extruder 1, there is, usually, used a biaxial extruder equipped with two or more screws, and the components are melted and mixed together while heating the interior of the cylinder at 250 C. to 350 C. Accompanying the melting and mixing, the polylactic acid starts depolymerizing, and the molecular weight of the polylactic acid starts decreasing.
(21) The molecular weight of the polylactic acid continues to decrease accompanying the melting and mixing, and there is obtained a lactide (dimer of lactic acid) that forms a basic unit of the polylactic acid. However, the lactide has a boiling point of 255 C. under the standard atmospheric pressure, which is in a boundary temperature region of gas-liquid separation where the gas cannot be trapped maintaining stability. That is, in a state where the lactide remains liquid, the lactide cannot be separated from the molten carrier resin effectively and stably. Therefore, the melt-kneaded product is introduced into the vent chamber 3 in which the pressure is maintained reduced in order to lower the boiling point of the lactide, to accelerate the gas-liquid phase conversion and to accelerate the gasification.
(22) Referring to
(23) A ceiling wall 17 of the vent chamber 3 has a tilted structure and a peep window 19 is fitted to the tilted portion thereof making it possible to observe, through the peep window 19 at all times, the interior of the vent chamber 3 and, specifically, the state of the first screw conveyer passage 11.
(24) Further, the lower end portion of the peep window 19 is stretching up to a portion on the outer side of the side wall 13 that is rising up from the first screw conveyer passage 11. A vessel 21 for receiving a refluxing liquid is provided on the lower side of the lower end portion of the peep window 19. The receiving vessel 21 is partitioned by the side wall 13 from the first screw conveyer passage 11 so that the refluxing liquid will not return to the screw conveyer passage 11.
(25) In the vent chamber 3 of the above structure, the screw conveyer passage 11 comprises a pair of first conveyer screws 23a and 23b that rotate in the same direction, a fall-down screw 25 suitably arranged over the one first conveyer screw 23a, and a cylinder wall (barrel) 27 that holds the first conveyer screws 23a and 23b.
(26) The cylinder wall 27 is the one that is extending from the cylinder wall of the extruder 1. Similarly, the first conveyer screws 23a and 23b are the ones that are extending from the screws in the extruder 1. Therefore, the molten mixture is conveyed from the extruder 1 toward the front of the surface of the paper in
(27) In the embodiment of
(28) As the return member, the fall-down screw 25 is selectively provided in the vent chamber 3 and is suitably arranged therein. The fall-down screw 25 is in engagement with the first conveyer screw 23a and rotates in a direction opposite to the conveyer screw 23a (but in the same direction at the nipping position).
(29) The pressure in the vent chamber 3 is reduced down to about 0.1 to about 8 kPaA by the operation of a vacuum pump 7. Due to a heater (not shown) provided in the cylinder wall 27, further, the interior of the first screw conveyer passage 11 is heated to about 250 C. to about 350 C. like in the cylinder portion in the extruder 1. Therefore, the lactide is gasified as it is formed by the depolymerization of the polylactic acid contained in the molten mixture that is introduced into the vent chamber 3 by the first conveyer screws 23a, 23b extending in the first screw conveyer passage 11. The gasified lactide is then introduced into the trapping apparatus 5 through the trapping tube 15.
(30) Here, the molten mixture conveyed by the screws contains a depolymerized product of polylactic acid having a high vapor pressure, and is introduced in a compressed state into the vent chamber 3 in which the pressure has been reduced. Therefore, the molten mixture expands in the vent chamber 3 and often forms resin masses 30 in a state of being floated over the first conveyer screws 23a and 23b. If the operation of the recovering apparatus is continued, therefore, the resin masses 30 are often formed continuously floating over the pair of first conveyer screws 23a and 23b in the vent chamber 3. The resin masses 30 are like a scab formed chiefly of the carrier resin. The resin masses 30 that grow large could clog and hinder the recovery of the lactide gas. Moreover, the scattered resin masses 30 could enter into the trapping apparatus 5 through the trapping tube 15, and could close the whole trapping tube 15. That is, the vent-up takes place.
(31) As will be understood from
(32) As described above, the fall-down screw 25 works as the return member for returning the resin masses 30 back to the first screw conveyer passage 11, whereby the resin masses 30 are suppressed from growing effectively preventing inconveniences caused by the growth of the resin masses 30.
(33) The turn of the fall-down screw 25 that is used as the return member may or may not be in synchronism with the turn of the first conveyer screws 23a and 23b.
(34) The vent-up could occur if the gasified lactide is cooled and liquefied (i.e., refluxed) again upon contacting to the peep window 19 and the like. However, the vent chamber 3 of the above-mentioned structure is capable of effectively preventing inconveniences caused by the refluxing liquid of lactide.
(35) That is, if the molten mixture containing the polylactic acid, depolymerization catalyst and carrier resin is introduced from the extruder 1 into the vent chamber 3 by the first screw conveyer passage 11 so as to continuously gasify the lactide, then liquid droplets 31 (i.e., refluxed liquid) are often formed being condensed on the surface of the peep window 19. The liquid droplets 31 that fall on the first screw conveyer passage 11 could form a liquid film so as to cover the surfaces of the first conveyer screws 23a, 23b running in the conveyer passage 11 or to cover the inner surfaces of the cylinder wall 27. Therefore, the molten mixture tends to undergo slipping and, as a result, the resin masses 30 are easily formed.
(36) With the vent chamber 3 of the structure shown in
(37) Further, the liquid droplets 31 that fall on the first screw conveyer passage 11 cause the gasification and liquefaction of the lactide in a recurring manner, accelerate the racemization of the lactide and, therefore, cause a degree in the optical purity of the lactide that is obtained. With the vent chamber 3 of the above-mentioned structure, however, the above inconvenience, too, can be effectively alleviated.
(38) It is desired that the peep window 19 is a double window as shown in
(39) The receiving vessel 21 for trapping the liquid droplets 31 (refluxing liquid) is provided in the bottom portion thereof with a recovering line 37 for recovering the refluxing liquid 31a that is collected in the receiving vessel 21. At an upper part of the side wall of the receiving vessel 21, there is provided a vacuum break/restore line 39 for holding a degree of vacuum in the vent chamber 3 or for breaking the vacuum therein. Due to this structure, the refluxing liquid 31a collected in the receiving vessel 21 can be recovered.
(40) The structure of the receiving vessel 21 is not limited to the one shown in
(41) The lactide gasified in the vent chamber 3 is introduced into the trapping apparatus 5 via the trapping tube 15 provided at the upper part of the side wall 13. Here, as shown in
(42) It is, further, desired that the inlet portion of the trapping tube 15, too, is provided with a receiving vessel 15a for receiving the refluxing liquid. That is, it is desired that the refluxing liquid liquefied in the trapping tube 15 is trapped by the receiving vessel 15a and is prevented from flowing down into the screw conveyer passage 11. The receiving vessel 15a, too, is provided with a vacuum break/restore line 15b and a recovering line 15c.
(43) In the trapping apparatus 5 to which the trapping tube 15 is linked, there are provided a gas-liquid separation column 51, a first condenser 53, a second condenser 55 and a chilling trap 57. Impurities are removed by gas-liquid separation from the gaseous product of lactide collected from the vent chamber 3, and the lactide is recovered in a highly pure form. That is, the gaseous product of lactide collected from the vent chamber 3 contains various low molecular compounds derived from oligomers of lactic acid and polymerization initiator contained in the polylactic acid or the carrier resin, in addition to containing the lactide. Therefore, these impurities must be removed.
(44) Concretely, the lactide recovered in a gaseous form is passed through the gas-liquid separation column (rectification column) 51 to remove high molecular oligomer components through the demister in the gas-liquid separation column. Thereafter, the lactide is introduced into the first condenser (heat exchanger) 53 where the lactide only is subjected to the phase conversion (phase change) so as to be recovered as liquid lactide.
(45) A proper heat-exchange temperature in the phase conversion varies depending on the degree of vacuum. Usually, under the standard atmospheric pressure, the lactide (L-lactide/D-lactide) has a boiling point and a melting point which are, respectively, 255 C. and 92 C. to 94 C. Therefore, the heat-exchange temperature is, preferably, 60 C. to 140 C. in a vacuum range of 0.1 KPaA to 8 KPaA. More preferably, the heat-exchange temperature is 80 C. to 90 C. in a vacuum range of 0.5 KPaA to 4 KPaA.
(46) If lower than 0.1 KPaA, for example, the degree of vacuum is so high that the resin masses are formed much, and the vent-up takes place easily. If higher than 8 KPaA, on the other hand, the degree of vacuum is so low that the boiling point of the lactide is not lowered to a sufficient degree, the lactide is not gasified to a sufficient degree, and the lactide recovering efficiency tends to decrease.
(47) If the heat-exchange temperature is lower than the above range, further, the low-boiling impurities tend to be liquefied, and the purity of the recovered lactide may decrease. If the heat-exchange temperature is higher than the above range, on the other hand, the lactide is not easily liquefied and, therefore, tends to be recovered at a decreased efficiency.
(48) Further, in order to recover the depolymerized product (lactide) of the polylactic acid in the gaseous form, it is desired that the facilities (gas-liquid separation column 51, first condenser 53, second condenser 55, etc.) in the trapping apparatus 5 are installed at positions higher than the vent chamber 3.
(49) The gas from which the oligomers are removed is cooled through the first condenser (heat exchanger) 53 down to about 80 C. whereby the desired lactide is liquefied and is recovered in the receiver 59. The remaining gas is cooled through the second condenser (heat exchanger) 55 down to about 5 C. whereby low-boiling low-molecular compounds are removed. Finally, the gas is cooled through the chilling trap 57 down to about 50 C., and the residual compounds, too, are removed in the form of a liquid.
(50) The refluxing liquid 31a collected in the receiving vessel 21 and the liquid collected in the bottom portion of the receiving vessel 15a provided in the trapping tube 15, can be directly discarded. Or, if there is no problem, these liquids can be introduced into the step of refining together with the liquid lactide recovered in the receiver 59.
(51) As described above, the molten resin composition containing the polylactic acid and the carrier resin is fed into the vent chamber 3 by using the first screw conveyer passage 11 (first conveyer screws 23a, 23b), and the lactide formed by the depolymerization of the polylactic acid is gasified in the vent chamber 3 and is recovered by the trapping apparatus 5. In this case, the volume of the molten resin composition conveyed by the first screw conveyer passage 11 decreases greatly as the lactide is gasified.
(52) In the present invention, the residue 65 of the molten resin composition (mostly, the carrier resin) from which the lactide has been removed in the form of a gas, is not discharged through the first screw conveyer passage 11 but is discharged through a carrier resin recovering chamber 4 provided under the vent chamber 3.
(53) That is, in the carrier resin recovering chamber 4 as shown in
(54) In the above-mentioned first screw conveyer passage 11, for instance, the cylinder wall 27 on the lower side of the first conveyer screws 23a, 23b is at least partly opened and is communicated with the second screw conveyer passage 60.
(55) The second conveyer passage 60 comprises a pair of second conveyer screws 60a and 60b that rotate in the same direction, and a cylinder wall 63 surrounding the second conveyer screws 60a and 60b.
(56) The second screw conveyer passage 60, as shown in
(57) That is, as shown in
(58)
(59) In the above-mentioned structure, the lactide formed by the depolymerization of the polylactic acid is gasified and is removed from the melt of resin on the first screw conveyer passage 11, and the resin mass (carrier resin) 65 which is the residue of the melt of resin falls from the first conveyer passage 11 on the second screw conveyer passage 60.
(60) In the above-mentioned method of the present invention, the carrier resin (i.e., material that could become a cause of resin masses 30) remaining on the first screw conveyer passage 11 is allowed to quickly fall on the second screw conveyer passage 60 dedicated to conveying the carrier resin, and is discharged. It is, therefore, made possible to effectively suppress the formation of the resin masses 30 on the first screw conveyer passage 11 and hence to effectively prevent the occurrence of the vent-up caused by the growth of the resin masses 30.
(61) In the present invention, it is desired that a diameter SD2 of the second conveyer screws 60a, 60b extending in the second screw conveyer passage 60 is set to be smaller than a diameter SD1 of the first conveyer screws 23a, 23b.
(62) That is, the molten carrier resin arrives at the second screw conveyer passage 60 and is conveyed by the second conveyer screws 60 and 60b. Thereafter, the molten carrier resin is melt-extruded from the discharge port 70 through the extruder 6 for discharging the carrier resin. To maintain the degree of vacuum in the vent chamber 3, in this case, the amount of the carrier resin must be secured so that the vacuum sealing is maintained in the extruder 6 for discharging the carrier resin. Here, by decreasing the diameter SD2 of the second conveyer screws 60a, 60b, the volume of gap decreases between the screws 60a, 60b and the surrounding cylinder wall. As a result, the vacuum sealing can be maintained by using the carrier resin in a decreased amount. As compared to the case where the second screw conveyer passage 60 has not been provided and the carrier resin is discharged from the first screw conveyer passage 11, therefore, it is made possible to depolymerize the polylactic acid with a resin composition that contains the carrier resin at a decreased ratio.
(63) According to the present invention as described above, it is desired that the diameter SD2 of the second conveyer screws 60a, 60b is smaller than the diameter SD1 of the first conveyer screws 23a, 23b. The diameter ratio SD2/SD1 is, more preferably, in a range of 0.25 to 0.90 and, further preferably, in a range of 0.35 to 0.80.
(64) If the diameter ratio SD2/SD1 is smaller than the above range, the amount of the carrier resin falling on the second screw conveyer passage 60 may surpass the amount that is discharged by the second conveyer screws 60a and 60b. The carrier resin can be discharged in an increased amount by increasing the rotational speed of the second conveyer screws 60a and 60b, as a matter of course. In this case, however, a too increased load may be exerted on the apparatus which, therefore, may be damaged or its service life may be shortened. If the diameter ratio SD2/SD1 is larger than the above range, on the other hand, the advantage of using the carrier resin in a decreased amount cannot be utilized to a sufficient degree and, besides, the vacuum sealing may become defective.
(65) In the invention described above, the second screw conveyer passage 60 comprises a pair of conveyer screws 60a and 60b. So far as the resin masses 65 can be conveyed and effectively discharged from the discharge port 70, however, there may be employed only one conveyer screw.
(66) In the embodiment shown in
(67) The carrier resin is discharged from the discharge port 70 provided at an end of the second screw conveyer passage 60 in the direction of feed. The carrier resin can be directly discarded but, as required, may be reused, i.e., may be mixed with the polylactic acid and may be fed again to the extruder 1.
(68) In carrying out the method of recovering lactide of the present invention, the recovering apparatus can be designed in a variety of different ways. As the return member for returning the resin masses 30 to the first screw conveyer passage 11, for instance, there can be used a member different from the fall-down screw 25.
(69) As shown in
(70) The fall-down screw 25 used as the return member and the rotary shaft 71 may rotate in, or out of, synchronism with the first conveyer screws 23a and 23b.
(71) It is, further, allowable to provide a plate-like return member or a point-contact return member so as to cover the upper side of the first conveyer screw 23a and/or 23b so will not to hinder the flow passage through which the lactide flows into the trapping tube 15 after having been gasified from the molten mixture conveyed by the screws 23a and 23b.
(72) Referring, for example, to
(73) In
(74) According to the present invention, as described above, it is made possible to effectively avoid the problem of vent-up caused by the resin masses 30 formed in the vent chamber 3 and, therefore, to stably operate the apparatus and to continuously recover the lactide of a high purity from the polylactic acid maintaining stability.
(75) Moreover, the amount of the carrier resin that is used can be greatly decreased (e.g., halved) as compared to the case where the first screw conveyer passage 11 is not closed at its one end and the carrier resin is discharged from the end thereof.
(76) In the present invention, further, it is also allowable to remove the resin masses 30 without providing the second screw conveyer passage 60 but by providing only the return member (see
DESCRIPTION OF REFERENCE NUMERALS
(77) 1: extruder 3: vent chamber 4: carrier resin recovering chamber 5: trapping apparatus 6: extruder for discharging the carrier resin 7: vacuum pump 11: first screw conveyer passage 15: trapping tube 19: peep window 21: receiving vessel 23a, 23b: first conveyer screws 25: fall-down screw 27: cylinder wall 51: gas-liquid separation column 53: first condenser 55: second condenser 60: second screw conveyer passage 60a, 60b: second conveyer screws 63: cylinder wall 65: molten resin residue (carrier resin mass) 70: discharge port