Method and device for producing crystallizable plastic material

Information

  • Patent Grant
  • 7291694
  • Patent Number
    7,291,694
  • Date Filed
    Friday, June 9, 2000
    24 years ago
  • Date Issued
    Tuesday, November 6, 2007
    16 years ago
Abstract
A method for manufacturing a crystallizable plastic material is disclosed. The process includes the step of melting an amorphous plastic material, pelletizing the material, crystallizing it and then post condensing the plastic material with the proviso that the plastic material is not subjected to heating after the melting step but prior to the crystallization step and then subjecting the plastic material to sieving after the crystallization step.
Description

This application is a 371 of PCT/CH00/00317 filed Jun. 9, 2000.


BACKGROUND OF THE INVENTION

The present invention relates to a procedure for manufacturing crystallizable plastic material, e.g., polyesters and the like, and in particular polyethylene terephthalate (PET), via post-melting phase crystallization and solid-phase post-condensation, and a device for executing the procedure.


The crystallization and post-condensation in the solid-phase (SSP) of polyesters obtained from a melt, in particular PET (polyethylene terephthalate), is generally known. In this case, the melted polyester (melting point 270° C. and [above] higher) is processed into cylindrical pellets, for example, while simultaneously cooled down to room temperature, and serves as an amorphous starting material for subsequent crystallization and post-condensation to PET. According to EP-A-379684, for example, crystallization takes place in two fluidized beds (combination of boiling and spouting beds) at temperatures of 140° C. to 180° C. Crystallization is followed by exposure to impact to dissolve agglomerates.


However, it is also known that crystallization can take place at a temperature of less than 140° C. and solid-state post-condensation can take place at a temperature exceeding 180° C. (e.g., according to the unpublished CH 02131/92-2).


EP-A-822214 describes a procedure in which a polymer material is extruded, pelleted and crystallized without cooling the melt to a temperature far below the crystallization temperature. In this case, a temperature of approx. 160° C. to 220° C. is maintained, and crystallization takes approx. 5-30 minutes. However, WO 97/23543 discloses this omission of strong cooling off during pelleting. Polyester is kept in a melt at approx. 270° C., and drips through a hole onto a hot (approx. 135° C.) metal plate, where crystallization has already taken place. A conventional SSP process then follows this for 24 hours at approx. 205° C. According to U.S. Pat. No. 5,510,454, the temperature of the plate that receives the drops can also measure 180° C.


Also known is a procedure for the simultaneous drying and crystallization of thermoplastics, e.g., PET according to WO94/25239, wherein plastic strands to be dried are quenched for at most 1.5 seconds to achieve a surface temperature of at least 100° C. This partial cooling of the plastic only reduces the crystallization time down to approx. 20 seconds at most.


In a device for manufacturing polyamides according to DE-A-19510698, a moving-bed reactor can be evacuated, wherein a vacuum pump can be provided with a separator for separating dust from the waste gas. However, solid foreign substances, dusts and the like are not reliably removed from the plastic material.


Further, U.S. Pat. No. 3,405,098 describes a procedure for preparing linear condensation polyesters for solid phase polymerization, wherein the melt is quickly quenched in order to obtain an essentially amorphous, solid polyester, which is subsequently heated to 150° C. to 200° C. again, in order to obtain a partially crystallized polyester, which is subsequently milled into fine particles, and classified using sieves. The polyester prepared in this way is then subjected to solid-phase polymerization in a fluidized bed.


SUMMARY OF THE INVENTION

One of the objects of the present invention is to further develop a procedure for manufacturing crystallizable plastic material, such as polyester or PET, in such a way as to achieve a higher reactivity in the SSP process through larger crystallites and improved surface crystal structure, and to reliably separate solid foreign substances from the plastic material after crystallization.


Another object of the present invention is to lower power consumption. This is accomplished based upon the features described in the claims.


Another object of the present invention is to provide a suitable device for executing the above procedure.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 shows a schematic view of an embodiment of the present invention.





DETAILED DESCRIPTION OF THE INVENTION

Preferred embodiments of the present invention are described in the claims.


The present invention shall be described in greater detail based upon the embodiment shown in FIG. 1. FIG. 1 shows a schematic view of the embodiment.


In particular, PET 1 exits a melt reactor (not shown) and enters a cutter 2 at a temperature of approx. 280° C. while being cooled and solidified.


The amorphous pellets 3 having a temperature of 140° C. to 180° C. generated in this way then pass to a fluidized bed 4 without further cooling, and subsequently to a sieve 5, which can be followed by a recirculating air sifter if required, in order to separate out dust and other foreign solids.


According to EP-A-379684, the fluidized bed 2 can also be a combination of boiling and spouted beds. If need be, the sieving process is followed by more crystallization (not shown).


The PET cleaned and crystallized passes in a conventional manner to a preheater 6 or directly to a shaft reactor 7, where the solid phase post-condensation into PET takes place, and only thereafter are the pellets cooled to room temperature in a cooler 8.

Claims
  • 1. A process for manufacturing crystallizable polyester comprising: (a) providing amorphous polyester from a melt reactor;(b) pelletizing the polyester;(c) crystallizing the polyester at a temperature of 140° C. to 180° C.; and(d) post-condensing the polyester;
  • 2. The process according to claim 1 wherein the polyester is polyethylene terephthalate.
  • 3. A device for manufacturing crystallizable polyester for executing a process according to claim 1, the device comprising a pelletizer, a fluidized bed (4) and a shaft reactor (7), wherein a sieve (5) is placed downstream from the fluidized bed (4).
  • 4. The device according to claim 3, wherein the polyester is polyethylene terephthalate.
  • 5. A process for manufacturing crystallizable polyester comprising: (a) providing amorphous polyester from a melt reactor;(b) crystallizing the polyester at 140° C. to 180° C.;(c) pelletizing the polyester; and(d) post-condensing the polyester;
  • 6. The process according to claim 5, wherein the temperature during the pelletization step and the sieving step is between 100° C. and 200° C.
  • 7. The process according to claim 5, wherein the temperature during the pelletization step and the sieving step is between 120° C. and 160° C.
  • 8. The process according to claim 5, wherein retention time during the crystallization step is approximately 1 to 40 seconds.
  • 9. The process according to claim 5, wherein retention time during the crystallization step is approximately 2 to 20 seconds.
  • 10. The process according to claim 5, wherein the sieving step is followed by a second crystallization step.
  • 11. The process according to claim 5, wherein the polyester is polyethylene terephthalate.
  • 12. A device for manufacturing crystallizable polyester, for executing a process according to claim 5, comprising a first crystallizer and a downstream cutter (2), wherein a sieve (5) is placed downstream from the cutter (2).
  • 13. The device according to claim 12, wherein a second crystallizer is placed downstream from the sieve (5).
  • 14. The device according to claim 12, wherein the polyester is polyethylene terephthalate.
Priority Claims (1)
Number Date Country Kind
199 38 583 Aug 1999 DE national
PCT Information
Filing Document Filing Date Country Kind 371c Date
PCT/CH00/00317 6/9/2000 WO 00 5/17/2002
Publishing Document Publishing Date Country Kind
WO01/12698 2/22/2001 WO A
US Referenced Citations (5)
Number Name Date Kind
4609721 Kirshenbaum et al. Sep 1986 A
4839969 Hahn Jun 1989 A
5424346 Sinclair Jun 1995 A
6436322 Fredl Aug 2002 B1
6524702 Betso et al. Feb 2003 B1
Foreign Referenced Citations (1)
Number Date Country
19919357 Nov 2000 DE