Title of Invention

CONTINUOUS PROCESS FOR PRODUCING POLY (TRIMETHYLENE TEREPHTHALATE)

Abstract

A continuous process for the production of poly(trimethylene terephthalate) comprising the steps of: (a) continuously feeding a liquid feed mixture to a flasher, the liquid feed mixture comprising a catalyst and at least one of bis-3-hydroxypropyl terephthalate and low molecular weight polyesters containing propylene groups from 1,3-propanediol and terephthalate groups, and the liquid feed mixture having a mole ratio of propylene groups to terephthalate groups of 1.1 to 2.2; (b) prepolymerizing the liquid reactants comprising the at least one of bis-3-hydroxypropyl terephthalate and low molecular weight polyesters in the flasher at 235° to 250°C and 40 to 80 mm of Hg; (c) continuously vaporizing by-products in the flasher and removing them from the flasher as a first stream of gaseous by-products comprising acrolein and allyl alcohol, and continuously withdrawing a liquid flasher reaction product having a mole ratio of propylene groups to terephthalate groups of less than 1.5 from the flasher; (d) continuously feeding the liquid flasher reaction product to a prepolymerizer, and continuously polymerizing the flasher reaction product in the prepolymerizer at 240° to 255°C and 5 to 30 mm of Hg to form a poly(trimethylene terephthalate) prepolymer and a second stream of gaseous by-products comprising acrolein and allyl alcohol; (e) continuously withdrawing the poly(trimethylene terephthalate) prepolymer from the prepolymerizer, the prepolymer having a relative viscosity of 5-7 and continuously removing the second stream of gaseous by-products from the prepolymerizer; (f) continuously feeding the poly(trimethylene terephthalate) prepolymer to a final polymerizer, and continuously polymerizing the poly(trimethylene terephthalate) prepolymer in the final polymerizer at 245° to 265°C and 0.5 to 3.0 mm Hg to form a higher molecular weight poly(trimethylene terephthalate) and a third stream of gaseous by-products comprising acrolein and allyl alcohol; (g) continuously withdrawing the higher molecular weight poly(trimethylene terephthalate) from the final polymerizer, the higher molecular weight poly(trimethylene terephthalate) having a relative viscosity of at least 17 and continuously removing the third stream of gaseous by-products from the final polymerizer; and (h) optionally (i) pelletizing the higher molecular weight poly(trimethylene terephthalate and/or (ii) forming the higher molecular weight poly(trimethylene terephthalate) into fibers, film or molded product.

Full Text

FORM 2 THE PATENTS ACT 1970 [39 OF 1970] COMPLETE SPECIFICATION [See Section 10] "CONTINUOUS PROCESS FOR PRODUCING POLY (TRIMETHYLENE TEREPHTHALATE)" E.I. DU PONT DE NEMOURS AND COMPANY, a corporation organized and existing under the laws of the State of Delaware, of 1007 Market Street, Wilmington, Delaware 19898, United States of America, The following specification particularly describes and ascertains the nature of the invention and the manner in which it is to be performed:- Field of the Invention The present invention relates to a continuous process for the production of poly(trimethylene terephthalate), which is also commonly referred to as poly(l,3-propylene terephthalate). The process of the invention can be used as part of a four-vessel process, the first vessel being either an ester exchanger for producing a mixture of bis-3-hydroxypropyl terephthalate and low molecular weight polymers of 1,3-propanediol and terephthalic acid having an average degree of polymerization of 15 or less from dimethylterephthalate and 1,3-propanediol or a reactor for producing the starting material from terephthalic acid and 1,3-propanediol. The second vessel is a flasher, the third vessel is a prepolymerizer, and the fourth vessel is a final polymerizer or finisher. Background of the Invention Continuous, four vessel processes for the production of poly(ethylene terephthalate) are known. For example, Sheller, U.S. Patent No. 3,438,942 discloses a process for the continuous production of poly(ethylene terephthalate) comprising ester exchange followed by three polycondensation steps. Also known are batch processes for the production of poly(trimethylene terephthalate). For example, Doerr et al., U.S. Patent No. 5,340,909 discloses the production of poly(trimethylene terephthalate) using either an ester exchange reaction starting with lower dialkyl terephthalate ester or direct esterification of terephthalic acid followed by a polycondensation reaction, both of which are carried out in batches using an autoclave. It would be highly desirable to provide a continuous, four-vessel process for the production of poly(trimethylene terephthalate). It would also be desirable to provide a continuous process for the production of poly(trimethylene terephthalate) in which the production of by-products, such as acrolein and allyl alcohol, is minimized, and in which the molecular weight of the final poly(trimethylene terephthalate) polymer is maximized. Summary of the Invention 1. A continuous process for the production of poly(rrimethylene terephthalate) comprising the steps of: (a) continuously feeding a liquid feed mixture to a flasher, the liquid feed mixture comprising a catalyst and at least one of bis-3-hydroxypropyl terephthalate and low molecular weight polyesters of 1,3-propanediol and terephthalic acid, and the liquid feed mixture having a mole ratio of propylene groups to terephthalate groups of 1.1 to 2.2; (b) continuously vaporizing and removing a first stream of gaseous by¬products from the flasher, and continuously withdrawing a liquid flasher reaction product having a mole ratio of propylene groups to terephthalate groups of less than about 1.5 from the flasher; (c) continuously feeding the liquid flasher reaction product to a prepolymerizer, and continuously polymerizing the flasher reaction product in the prepolymerizer to form a poly(trimethylene terephthalate) prepolymer and a second stream of gaseous by-products; (d) continuously withdrawing the poly(trimethylene terephthalate) prepolymer from the prepolymerizer, the prepolymer having a relative viscosity of at least about 5; (e) continuously feeding the poly(trimethylene terephthalate) prepolymer to a final polymerizer, and continuously polymerizing the poly(trimethylene terephthalate) prepolymer to form a higher molecular weight poly(trimethylene terephthalate) and a third stream of gaseous by-products; and (f) continuously withdrawing the higher molecular weight poly(trimethylene terephthalate) from the final polymerizer, the higher molecular weight poly(trimethylene terephthalate) having a relative viscosity of at least about 17. Description of the Drawings Figure 1 is a schematic representation of an apparatus useful in carrying out tie process of the invention. Detailed Description of the Preferred Embodiments The process of the invention is part of a continuous, four-vessel, four-stage rocess for the production of poly(trimethylene terephthalate). The first stage in the rocess is either an ester exchange or direct esterification reaction, depending upon whether the starting material for the process is dimethylterephthalate or terephthalic cid. The second stage is the rapid removal of 1,3-propanediol in a flasher, the third tage is a prepolymerization, and the fourth stage is a final polymerization. Production of Feed Materials The feed material for the flasher may be produced either by ester exchange rom dimethylterephthalate and 1,3-propanediol or by direct esterification from terephthalic acid and 1,3-propanediol. Both processes yield bis-3-hydroxypropyl terephthalate (referred to as "monomer") and low molecular weight polyesters of 1,3-propanediol and terephthalic acid having an average degree of polymerization of 15 or less (referred to as "oligomers"). As shown in Figure 1, reaction vessel 10 is a source of monomer and/or . oligomers, which are fed to flasher 12. Reaction vessel 10 can be either an ester exchange reactor or a direct esterification reactor. Whether the monomer/oligomer feed mixture is produced by direct esterification from terephthalic acid or ester exchange from dimethylterephthalate, a catalyst is added prior to the esterification or transesterification reaction. Catalysts useful in the ester exchange process include organic and inorganic compounds of titanium, lanthanum, and zinc. Titanium catalysts, such as tetraisopropyl titanate and tetraisobutyl titanate are preferred and are added to the 1,3-propanediol in an amount sufficient to yield 20 to 90 ppm of titanium by weight based on the finished polymer. These levels produce relatively low unreacted dimethylterephthalate in the ester exchange reaction (less than 5% by weight based on the total weight of the exit stream from the ester exchange), give reasonable reaction rates in the prepolymerization and final polymerization steps, and produce polymer with CIELAB b* color of less than 8'. Another useful ester exchange catalyst is lanthanum acetate, which may be added in an amount sufficient to yield 125 to 250 ppm of lanthanum by weight based on the finished polymer. Following the ester exchange reaction, the lanthanum is deactivated by the addition of phosphoric acid in an amount sufficient to yield 10 to 50 ppm of phosphorus by weight based on the finished polymer. Tetraisopropyl titanate or tetraisobutyl titanate is then added as a polycondensation catalyst in an amount sufficient to yield 10 to 50 ppm of titanium by weight based on the finished polymer. Amounts of other ester exchange catalysts are adjusted to give the same effect as the 20 to 90 ppm of titanium. Catalysts useful in the direct esterification process include organo-titanium and organo-tin compounds, which are added to the 1,3-propanediol in an amount sufficient to yield at least 20 ppm of titanium, or at least 50 ppm of tin, respectively, by weight based on the finished polymer. Additional catalyst may be added to the monomer/oligomer mixture after the ester exchange or direct esterification reaction and prior to prepolymerization. Whether the monomer/oligomer feed mixture is produced by direct esterification from terephthalic acid or ester exchange from dimethylterephthalate, the mole ratio of propylene groups to terephthalate groups is maintained at about 1.1 to 2.2, preferably about 1.4 to 1.8, and more preferably about 1.5 entering the flasher. 2. Flasher As shown in Figure 1, the monomer/oligomer mixture is pumped from the ester exchanger. or direct esterification reactor to flasher 12 by means of a temperature-controlled feed line 11 equipped with pumps and filters. In the feed lines, the monomer/oligomer mixture is maintained at a temperature of about 215° to 250°C. The flasher is a jacketed and heated vessel with an internal heater. The internal heater heats and vaporizes the excess 1,3-propanediol in the feed material. 1,3-propanediol is removed through vapor line 13 connected to a vacuum source and then condensed. In the flasher, the monomer/oligomer mixture is maintained at a temperature of about 235° to 250°C, preferably about 240° to 245°C, and more preferably about 245°C. The pressure in the flasher is maintained at about 40 to 80 mm of Hg, preferably about 45 to 75 mm Hg, and more preferably about 50 to 70 mm Hg. In the flasher, the monomer/oligomer mixture reacts to form a liquid flasher reaction product comprising a low molecular weight trimethylene terephthalate polymer and releasing 1,3-propanediol as a by-product. The excess 1,3-propanediol is vaporized and continuously removed from the liquid reactants, lowering the 1,3-propanediol to dimethylterephthalate mole ratio to less than about 1.5, preferably less than about 1.3, in the liquid flasher reaction product. The excess 1,3-propanediol that is removed from the flasher can be condensed by means of spray condenser 14. Vapors from vapor line 13 pass into a vertical condenser, where they are sprayed with condensed 1,3-propanediol that has been cooled to a temperature of less than 60°C, preferably less than 50°C. The condensed 1,3-propanediol vapors from flasher 12, together with the 1,3-propanediol spray, flow into hotwell 15 located beneath condenser 14, where they are combined with additional 1,3-propanediol. A portion of the liquid mixture in hotwell 14 is pumped through a cooler to the top of the condenser for use as the condensing spray. The condensed vapors from flasher 1? are combined with the condensed vapors from prepolymerizer 17 in hotwell 15. 3. Prepolymerization As shown in Figure 1, the flasher reaction product is fed via temperature-controlled feed line 16 to prepolymerizer 17. Prepolymerizer 17 performs the initial polymerization step,which involves removing excess 1,3-propanediol the product viscosity by building longer chain molecules of polymer. The prepolymerizer is a jacketed and heated vessel with an internal agitator. The agitator provides agitation and creates liquid/vapor surface area for 1,3-propanediol removal. The temperature of liquid reactants in the prepolymerizer is maintained at about 240° to 255°C, preferably about 245° to 250°C, and more preferably about 250°C. The pressure in the prepolymerizer is maintained at about 5 to 30 mm of Hg, preferably about 10 to 20 mm of Hg, and more preferably about 15 mm of Hg. The excess 1,3-propanediol is removed through vapor line 18 connected to a vacuum, source and then condensed. One method foi condensing the 1,3,-propanedial vapors from the prepolymerizer is by means of spray condenser 19 similar to that described above for condensing 1,3-propanediol vapors from the flasher. The condensed vapors from prepolymerizer 17 are combined with the condensed vapors from flasher 12 in hotwell 15. The condensed 1,3-propanediol vapors exiting the flasher and prepolymerizer typically contain other reaction by-products such as acrolein and allyl alcohol. It is desirable that the production of by-products such as acrolein and allyl alcohol be minimized because both of these compounds are highly toxic and cause irritation to the eyes and mucous membranes. According to the process of the invention, the amount of acrolein contained in the combined condensed 1,3-propanediol streams exiting the flasher and prepolymerizer is no greater than 100 ppm by weight of condensate, preferably no greater than 60 ppm, and more preferably no greater than 40 ppm. The amount of allyl alcohol contained in the combined condensed 1,3-propanediol streams exiting the flasher and prepolymerizer is no greater than 600 ppm by weight of condensate, preferably no greater than 400 ppm, and more preferably no greater than 250 ppm. Relative viscosity is an indicator of molecular weight. Relative viscosity, often referred to as "LRV," is the ratio of the viscosity of a solution of 4.75 grams of poly(trimethylene terephthalate) in 100 grams of solution to the viscosity of the solvent itself. The solvent used herein for measuring relative viscosity is hexafluoroisopropanol containing 100 ppm sulfuric acid, and the measurements are made at 25°C. The poly(trimethylene terephthalate) prepolymer that is withdrawn from the prepolymerizer has a relative viscosity of at least about 5, preferably about 5.5 to 7. The residence or hold-up time in the prepolymerizer typically ranges from about 30 to 90 minutes. 4. Final Polymerization As shown in Figure 1, the liquid reaction product from prepolymerizer 17 is fed via temperature-controlled feed line 20 to final polymerizer or finisher 21. The major purpose of finisher 21 is to increase the molecular chain length or viscosity of the polymer. This is accomplished by using heat, agitation, vacuum and catalyst. It is desirable that the molecular weight of the finished polymer be maximized, so that further processing, e.g., solid state polymerization, can be avoided prior to fiber spinning or other forming operation. The finisher is normally a horizontal cylindrical vessel surrounded by a jacket containing a heating medium, such as Dowtherm vapor. Prepolymer from prepolymerizer 17 flows through an inlet into the finisher. An agitator generates large surface areas of thin films of polymer to enhance the mass transfer of 1,3-propanediol from the polymer. The temperature of the liquid reactants in the finisher is maintained at about 245° to 265°C, preferably about 250° to 260°C, and more preferably about 255°C. The pressure in the finisher is maintained at about 0.5 to 3;0 mm Hg. Finished polymer is removed from the finisher through an outlet by means of a pump. The relative viscosity of the poly(trimethylene terephthalate) exiting the finisher is at least about 17, preferably at least about 35, more preferably at least about 40, more preferably at least about 45, and most preferably at least about 50. When correlated to intrinsic viscosity measurements in 60/40 weight percent phenol/1,1,2,2-tetrachloroethane following ASTM D 4603-96, these relative viscosities correspond to intrinsic viscosities of 0.55 dl/g, 0.85 dl/g, 0.91 dl/g, 0.96 dl/g, and 1.0 dl/g, respectively. The viscosity of the finished polymer may be controlled by adjusting finisher pressure or other variables. The residence or hold-up time in the finisher is typically about 1 to 2 hours. 1,3-Propanediol and other gaseous by-products are removed from the finisher through vapor line 22 connected to a vacuum source and then condensed. One nethod for condensing the 1,3-propanediol vapors from the finisher is by means of spray condenser 23 similar to that described above for condensing 1,3-propanediol vapors from the flasher and prepolymerizer. The condensed vapors from finisher 21 are collected in hotwell 24. According to the present invention, the amount of acrolein contained in the condensed 1,3-propanediol stream exiting the finisher is no greater than 200 ppm by weight of condensate, preferably no greater than 100 ppm, and more preferably no greater than 70 ppm. The amount of allyl alcohol contained in the condensed 1,3-propanediol stream exiting the finisher is no greater than 3000 ppm, preferably no greater than 2500 ppm, and more preferably no greater than 1000 ppm. The finished polymer may be pelletized or fed directly to a forming operation, such as fiber spinning, film formation or molding operation. Fibers made from the poly(trimethylene terephthalate) produced by the process of the invention have properties which make them useful in various textile applications, including the manufacture of carpet or apparel. 4. Additives Various additives may be used in the process of the invention. These include color inhibitors, such as phosphoric acid, delustrants, such as titanium dioxide, dyeability modifiers, pigments and whiteners. If separate ester exchange and polymerization catalysts are used, phosphoric acid (H3PO4) or other color inhibitors may be added to minimize or prevent the color forming property of the ester exchange catalyst. EXAMPLES Poly(trimethylene terephthalate) was prepared using an apparatus of the type indicated in the drawing, including an ester exchanger, a flasher, a prepolymerizer and a finisher. In Examples 1-8, a 94.1 lb./hr (42.7 kg/hr) stream of dimethylterephthalate was preheated to a temperature of 185°C and continuously mixed with a 55.3 lb./hr (25.1 kg/hr) stream of catalyzed 1,3-propanediol which Was also preheated to a temperature of 185°C, to form a mixture having a mole ratio of 1.5 moles of 1,3-propanediol per mole of dimethylterephthalate. In Example 9, the throughput was lowered to 51.4 lb./hr (23.3 kg/hr) of dimethyltereph-thalate and 40.3 lb./hr (18.3 kg/hr) of catalyzed 1,3-propanediol which were combined to form a mixture having a mole ratio of 2.0 moles of 1,3-propanediol per mole of dimethylterephthalate. In Example 10, the throughput was lowered still further to 38.2 lb./hr (17.3 kg/hr) of dimethylterephthalate and 30.0 lb/hr (13.6 kg/hr) of catalyzed 1,3-propanediol which were combined to form a mixture having a mole ratio of 2.0 moles of 1,3-propanediol per mole of dimethylterephthalate. The catalyst was tetraisopropyl titanate (Tyzor® TPT, DuPont Performance Chemicals). In Examples 1-8, the tetraisopropyl titanate was added to the 1,3-propanediol in an amount sufficient to yield 30-60 ppm by weight of titanium based on the weight of poly(trimethylene terephthalate) formed in the process. In Examples 9 and 10, the catalyst level was raised to 70 ppm of titanium. The dimethylterephthalate/catalyzed 1,3-propanediol mixture was fed into the base of an ester exchanger, where the pressure at the base of the ester exchanger was maintained at 825 to 900 mm Hg. In Examples 1-8, the temperature of the liquid reactants in the ester exchanger was maintained at 230°C, and in Examples 9 and 10, the temperature of liquid reactants in the ester exchanger was maintained at 237°C and 239°C, respectively. The pressure at the top of the ester exchange column was atmospheric. In the ester exchanger, the 1,3-propanediol reacted with the dimethylterephthalate to form bis-3-hydroxypropyl terephthalate monomer and low molecular weight oligomers of 1,3-propanediol and terephthalic acid, liberating methanol vapor, which was continuously removed from the top of the ester exchanger. The monomer/oligomer mixture was continuously removed from the base of the ester exchanger and fed to the inlet of a flasher. In the flasher, the monomers and oligomers reacted to form a low molecular weight trimethylene terephthalate polymer, liberating 1,3-propanediol vapor. The 1,3-propanediol vapor and other gaseous by-products were removed from the top of the flasher and condensed. The low molecular weight trimethylene terephthalate polymer was continuously withdrawn from the flasher and fed to the inlet end of a prepolymerizer. In the prepolymerizer, the monomers and oligomers further reacted to form a higher molecular weight poly(trimethylene terephthalate) prepolymer, liberating 1,3-propanediol vapor. The 1,3-propanediol vapor and other gaseous by-products were removed from the top of the prepolymerizer, condensed and combined with the condensates from the flasher. The poly(trimethylene terephthalate) prepolymer was continuously withdrawn from the prepolymerizer and fed to the inlet end of a finisher vessel. The temperature of the liquid reactants in the finisher was maintained at 255° to 260°C. In the finisher, the poly(trimethylene terephthalate) prepolymer reacted to form an even higher molecular weight polymer, liberating additional 1,3-propanediol vapor. The 1,3-propanediol vapor and other gaseous by-products were continuously removed from the finisher. The poly(trimethylene terephthalate) was continuously removed from the finisher and pelletized. The conditions and results for the continuous polymerization are set forth in Tables I, II and III. In Examples 9 and 10, the levels of polymer and hold-up times in the finisher were reduced, resulting in lower by-product formation and higher relative viscosity (LRV). In the Tables, the acrolein and allyl alcohol levels are given in parts per million (ppm) by weight based on the combined condensates that are removed from the flasher and prepolymerizer and the condensates that are removed from the finisher, respectively. The dipropylene glycol (DPG) levels are given as a weight percent based on the total prepolymer or finished polymer that is removed from the flasher, prepolymerizer and finisher, respectively. The speed of the agitator in the finisher is given in revolutions per minute (RPM). The amount of carboxyl end groups (COOH) in the finished polymer is given in microequivalents per gram based on the total weight of the finished polymer. The level of catalyst is given as parts per million (ppm) by weight of titanium in the finished polymer. TABLE II TABLE I We Claim: 1. A continuous process for the production of poly(trimethylene terephthalate) comprising the steps of: (a) continuously feeding a liquid feed mixture to a flasher, the liquid feed mixture comprising a catalyst and at least one of bis-3-hydroxypropyl terephthalate and low molecular weight polyesters containing propylene groups from 1,3-propanediol and terephthalate groups, and the liquid feed mixture having a mole ratio of propylene groups to terephthalate groups of 1.1 to 2.2; (b) prepolymerizing the liquid reactants comprising the at least one of bis-3-hydroxypropyl terephthalate and low molecular weight polyesters in the flasher at 235° to 250°C and 40 to 80 mm of Hg; (c) continuously vaporizing by-products in the flasher and removing them from the flasher as a first stream of gaseous by-products comprising acrolein and allyl alcohol, and continuously withdrawing a liquid flasher reaction product having a mole ratio of propylene groups to terephthalate groups of less than 1.5 from the flasher; (d) continuously feeding the liquid flasher reaction product to a prepolymerizer, and continuously polymerizing the flasher reaction product in the prepolymerizer at 240° to 255°C and 5 to 30 mm of Hg to form a poly(trimethylene terephthalate) prepolymer and a second stream of gaseous by-products comprising acrolein and allyl alcohol; (e) continuously withdrawing the poly(trimethylene terephthalate) prepolymer from the prepolymerizer, the prepolymer having a relative viscosity of 5-7 and continuously removing the second stream of gaseous by-products from the prepolymerizer; (f) continuously feeding the poly(trimethylene terephthalate) prepolymer to a final polymerizer, and continuously polymerizing the poly(trimethylene terephthalate) prepolymer in the final polymerizer at 245° to 265°C and 0.5 to 3.0 mm Hg to form a higher molecular weight poly(trimethylene terephthalate) and a third stream of gaseous by-products comprising acrolein and allyl alcohol; (g) continuously withdrawing the higher molecular weight poly(trimethylene terephthalate) from the final polymerizer, the higher molecular weight poly(trimethylene terephthalate) having a relative viscosity of at least 17 and continuously removing the third stream of gaseous by-products from the final polymerizer; and (h) optionally (i) pelletizing the higher molecular weight poly(trimethylene terephthalate and/or (ii) forming the higher molecular weight poly(trimethylene terephthalate) into fibers, film or molded product. The process as claimed in claim 1, wherein the temperature of liquid reactants comprising the at least one ofbis-3-hydroxypropyl terephthalate and low molecular weight polyesters in the flasher is maintained at 240° to 245°C, and the pressure in the flasher is maintained at 45 to 75 mm of Hg. The process as claimed in anyone of the preceding claims, wherein the temperature of liquid reactants comprising the liquid flasher reaction product in the prepolymerizer is maintained at 245° to 250°C, and the pressure in the prepolymerizer is maintained at 5 to 30 mm of Hg. 4. The process as claimed in anyone of the preceding claims, wherein the temperature of liquid reactants comprising the poly(trimethylene terephthalate) prepolymer in the final polymerizer is maintained at 250° to 260°C, and the pressure in the final polymerizer is maintained at 0.8 to 2.5 mm Hg. 5. The process as claimed in any of the preceding claims, wherein the poly(trimethylene terephthalate) that is withdrawn from the final polymerizer has a relative viscosity of at least 35. 6. The process as claimed in any of the preceding claims, wherein the poly(trimethylene terephthalate) that is withdrawn from the final polymerizer has a relative viscosity of at least 40. 7. The process as claimed in any of the preceding claims, wherein the poly(trimethylene terephthalate) that is withdrawn from the final polymerizer has a relative viscosity of at least 50. 8. The process as claimed in any of the preceding claims, wherein the first and second streams of condensed by-products contain not more than 100 ppm of acrolein and not more than 600 ppm of allyl alcohol. 9. The process as claimed in claim 8, wherein the first and second streams of by-products contain not more than 40 ppm of acrolein and not more than 250 ppm of allyl alcohol. 10. The process as claimed in any of the preceding claims, wherein the third stream of gaseous by-products contains not more than 200 ppm of acrolein and not more than 3000 ppm of allyl alcohol. 11. The process as claimed in claim 10, wherein the third stream of gaseous by-products contains not more than 70 ppm of acrolein and not more than 1000 ppm of allyl alcohol. 12. The process as claimed in any of the preceding claims, wherein the liquid feed mixture is prepared by the direct esterification of terephthalic acid and 1 ,3-propanediol using a titanium catalyst. 13. The process as claimed in claim 12, wherein the catalyst is tetraisopropyl titanate in an amount sufficient to yield 20 to 90 ppm of titanium by weight based on the higher molecular weight poly(trimethylene terephthalate). 14. The process as claimed in claim 12, wherein the liquid feed mixture is prepared by the ester exchange of dimethylterephthalate and 1,3-propanediol. 15. The process as claimed in any of the preceding claims wherein it further comprises (a) optionally palletizing the higher molecular weight poly(trimethylene terephthalate) and (b) forming the higher molecular weight poly(trimethylene terephthalate) into fibers, film or molded product, wherein solid state polymerization is not carried out prior to the forming. Dated this 8th Day of July, 2002. [RANJNA MEHTA-DUTT] OF REMFRY & SAGAR ATTORNEY FOR THE APPLICANTS

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