Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
  • C08G63/78—Preparation processes
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
  • C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
  • C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
  • C08G63/16—Dicarboxylic acids and dihydroxy compounds
  • C08G63/18—Dicarboxylic acids and dihydroxy compounds the acids or hydroxy compounds containing carbocyclic rings
  • C08G63/199—Acids or hydroxy compounds containing cycloaliphatic rings
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
  • C08G63/66—Polyesters containing oxygen in the form of ether groups
  • C08G63/668—Polyesters containing oxygen in the form of ether groups derived from polycarboxylic acids and polyhydroxy compounds
  • C08G63/672—Dicarboxylic acids and dihydroxy compounds
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
  • C08G63/68—Polyesters containing atoms other than carbon, hydrogen and oxygen
  • C08G63/685—Polyesters containing atoms other than carbon, hydrogen and oxygen containing nitrogen
  • C08G63/6854—Polyesters containing atoms other than carbon, hydrogen and oxygen containing nitrogen derived from polycarboxylic acids and polyhydroxy compounds
  • C08G63/6856—Dicarboxylic acids and dihydroxy compounds
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
  • C08G63/78—Preparation processes
  • C08G63/82—Preparation processes characterised by the catalyst used
  • C08G63/85—Germanium, tin, lead, arsenic, antimony, bismuth, titanium, zirconium, hafnium, vanadium, niobium, tantalum, or compounds thereof
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
  • C08G63/78—Preparation processes
  • C08G63/82—Preparation processes characterised by the catalyst used
  • C08G63/826—Metals not provided for in groups C08G63/83 - C08G63/86
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
  • C08G63/78—Preparation processes
  • C08G63/82—Preparation processes characterised by the catalyst used
  • C08G63/83—Alkali metals, alkaline earth metals, beryllium, magnesium, copper, silver, gold, zinc, cadmium, mercury, manganese, or compounds thereof
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
  • C08G63/78—Preparation processes
  • C08G63/82—Preparation processes characterised by the catalyst used
  • C08G63/84—Boron, aluminium, gallium, indium, thallium, rare-earth metals, or compounds thereof

Definitions

• This invention relates to the preparation of polyesters, and more particularly to the preparation of poly(1 ,4-cyclohexane-dicarboxylates).
• Poly(1 ,4-cyclohexanedicarboxylates) such as poly(1 ,4-cyclohexanedimethyl- 1 ,4-cyclohexanedicarboxylate), hereinafter sometimes designated "PCCD" for brevity, are known polyesters; reference is made, for example, to US Patent 2,891 ,930.
• PCCD is characterized by such advantageous properties as crystallinity and resistance to weathering under conditions of exposure to ultraviolet radiation. These properties have increased interest in commercialization in recent years.
• DMCD dimethyl ester
• the proportion of trans isomer in DMCD as typically supplied is on the order of 99%.
• isomerization can take place with an increase in the level of the cis isomer, decreasing crystallinity.
• the CHDM reagent is normally about 70% trans, but no isomerization of those molecules takes place during product formation.
• the present invention provides various improvements in the process for preparation of poly(1 ,4-cyclohexanedicarboxylates). These improvements may be employed individually or in various combinations, and when so employed make it possible to produce a rapidly crystallizing polymer and/or a polymer of high molecular weight.
• poly(1 ,4-cyclohexane-dicarboxylates) are prepared by the reaction of at least one relatively non-volatile diol with a 1 ,4-cyclohexanedicarboxylic acid ester in the presence of a transesterification catalyst, employing at least one of the following options:
• polyesters produced by the method of this invention are 1 ,4- cyclohexanedicarboxylates, characterized by the presence of structural units of the formula
• R is an alkyl radical derived primarily from at least one relatively nonvolatile diol HO-R-OH. It is most often a homopolyester, but as noted hereinafter, it may also be a copolyester or a copolyesteramide.
• the 1 ,4-cyclohexanedicarboxylic acid esters employed in the method of this invention are known compounds. Suitable 1 ,4-cyclohexanedicarboxylic acid esters include, but are not limited to, C,_ 6 alkyl esters, aromatic esters, and substituted aromatic esters, particularly alkyl-substituted aromatic esters.
• Alkyl-substituted aromatic groups within the context of the present invention refer to aromatic groups bearing at least one C ⁇ e alkyl substituent.
• Preferred aromatic groups are phenyl, tolyl, xylyl, and trimethylphenyl.
• Particularly preferred 1 ,4-cyclohexanedicarboxylic acid esters are phenyl esters and C- ) . 6 alkyl esters.
• the ester is dimethyl-1 ,4- cyclohexanedicarboxylate (DMCD).
• DMCD undergoes a transesterification reaction with at least one relatively non-volatile diol.
• relatively non-volatile diols are those having a boiling point (at atmospheric pressure) above the initial condensation temperature of a series of progressively increasing temperatures below 265°C under which conditions the transesterification reaction of the present invention is performed.
• the relatively non-volatile diol or mixture of relatively non-volatile diols has a boiling point above about 220°C, more preferably above about 240°C, and most preferably above about 260°C.
• the relatively non-volatile diol or mixture of relatively non-volatile diols has a boiling point at atmospheric pressure of above about 250°C .
• Suitable diols are known in the art and include CHDM.
• CHDM CHDM
• the invention will frequently be described herein with reference to CHDM as the diol; however, it should be understood that other relatively non-volatile diols may be substituted for CHDM or combined with CHDM as appropriate.
• Suitable catalysts for transesterification are well-known in the art and include organometallic compounds containing at least one metal selected from the group consisting of titanium, zirconium, tin, germanium, gallium, zinc, iron, manganese, cobalt, hafnium, vanadium, iridium, lanthanum, cerium, lithium, calcium, magnesium, barium, nickel, and aluminum. Only one kind of the above-listed catalysts may be employed, or two or more kinds thereof may be suitably mixed and employed.
• the catalyst is a tetraalkyl titanate such as tetraisopropyl titanate, hereinafter sometimes "TPT".
• Proportions thereof are in the range of about 0.005-0.5 and more preferably in the range of about 0.02-0.12 mole percent based on 1 ,4- cyclohexanedicarboxylic acid ester. It may, on occasion, be advantageous to introduce the catalyst in stages, with up to about 50% thereof being present at the initiation of the transesterification reaction and the balance being added subsequently, most often after about 30-50% of the total reaction time.
• the catalyst may be introduced into the reaction mixture by any means known in the art. Often it is convenient to add the catalyst either neat or as a solution in an inert solvent.
• Solvents and diluents are not necessary according to the invention and are preferably not present other than in trace amounts. Subatmospheric reaction pressures may be employed.
• the poly(1 ,4-cyclohexanedicarboxylate) to be a copolyester of a type incorporating "soft-blocks" derived from polyethers. This may be done by incorporating in the transesterification reaction mixture at least one relatively non-volatile bis(hydroxy-terminated) polyether such as, but not limited to, poly(ethylene glycol), polypropylene glycol), poly(butylene glycol) and their copolymers such as bis(hydroxy-terminated) poly(ethylene oxide-co-propylene oxide).
• at least one relatively non-volatile bis(hydroxy-terminated) polyether such as, but not limited to, poly(ethylene glycol), polypropylene glycol), poly(butylene glycol) and their copolymers such as bis(hydroxy-terminated) poly(ethylene oxide-co-propylene oxide).
• the copolyester consists essentially of diol units derived from 1 ,4-cyclohexanedimethanol and diol units derived from at least one relatively non-volatile bis(hydroxy-terminated) polyether. It is further within the scope of the invention for the poly(1 ,4-cyclohexanedicarboxylate) to be a copolyesteramide of a type incorporating "soft-blocks" derived from relatively non-volatile bis(amine- terminated) polyethers.
• the transesterification reaction mixture may be done by incorporating in the transesterification reaction mixture at least one bis(amine-terminated)- polyalkylene oxide, such as, but not limited to, bis(amine-terminated)- polyethylene oxide, -polypropylene oxide, -polybutylene oxide, and their copolymers such as bis(amine-terminated) poly(ethylene oxide-co-propylene oxide).
• the copolyesteramide consists essentially of diol units derived from 1 ,4-cyclohexanedimethanol and diamine units derived from at least one relatively non-volatile bis(amine-terminated) polyether.
• thermal stabilizers are non-reactive stabilizers including those which will not themselves undergo transesterification with the poly(1 ,4-cyclohexanedi-carboxylate) product.
• thermal stabilizers include 1 ,3,5-trimethyl-2,4,6-tris(3,5-di-tert-butyl-4- hydroxybenzyl)benzene.
• a sufficient amount of stabilizer is used to prevent significant degradation of said polyether and polyether-containing copolyester under the reaction conditions.
• 0.1-2.0 wt. % stabilizer and more preferably 0.2-1.0 wt. % stabilizer based on polyether is employed.
• the poly(1 ,4-cyclohexanedicarboxylate) to be a copolyesteramide of the type disclosed in copending, commonly owned application Serial No. 09/075,914. This may be done by incorporating in the transesterification reaction mixture at least one non-polyether-containing diamine such as hexamethyienediamine or a bisesteramide derived therefrom, such as hexamethylenebis(4-carbomethoxy-cyclohexylcarboxamide).
• the reaction of at least one relatively non-volatile diol with 1 ,4-cyclohexanedi-carboxylic acid ester is conducted at a series of progressively increasing temperatures, normally starting in the range of about 150-160°C and increasing over the course of the reaction to a maximum level.
• the molar ratio of 1 ,4-cyclohexanedicarboxylic acid ester to relatively non-volatile diol or mixture of relatively non-volatile diols is most often in the range of about 1.001-1.01 :1.
• a diol volatile under the transesterification reaction conditions is evolved during the transesterification between relatively non-volatile diol or mixture of relatively non-volatile diols with 1 ,4-cyclohexanedicarboxylic acid ester. Said volatile diol is removed under the reaction conditions to drive the transesterification equilibrium to polymer.
• the 1 ,4-cyclohexanedicarboxylic acid ester is DMCD
• methanol is evolved during the reaction with the at least one relatively non-volatile diol, and the methanol is removed by distillation to facilitate formation of poly(1 ,4-cyclohexanedicarboxylate).
• the maximum temperature should be below 265°C for optimum molecular weight increase.
• the maximum temperature is 255°C; most preferably, it is 253°C.
• a residence time of the reaction mixture at temperatures above 250°C is maintained in the range of 40-120 minutes, and more preferably in the range of 80-120 minutes.
• the optimum residence time range of the reaction mixture at temperatures above 250°C will depend on factors including the surface-to-volume ratio of the reaction equipment and the rate of surface renewal in said equipment. By employing the specified temperatures, it is possible to obtain a product of maximum Mw, typically above 70,000, and with a high degree of crystallinity and capability of rapid crystallization, as evidenced by a Tc frequently above 175°C.
• the initial stage of the transesterification reaction is conducted in the presence of at least one C 2 . 6 aliphatic diol.
• Suitable C 2 . 6 aliphatic diols are those which have a boiling point at atmospheric pressure less than the boiling point at atmospheric pressure of the relatively nonvolatile diol or mixture of relatively non-volatile diols.
• Preferred C 2 . 6 aliphatic diols include ethylene glycol, diethylene glycol, neopentylene glycol, and 1 ,4- butanediol.
• the C 2 . 6 aliphatic diol is normally introduced at the beginning of the reaction.
• the molar ratio of the relatively non-volatile diol or mixture of relatively non-volatile diols to 1 ,4-cyclohexanedicarboxylic acid ester may be somewhat higher than otherwise; for example, in the range of about 1.025-1.15:1.
• the C 2 . 6 aliphatic diol is present in the amount of about 3- 25 and preferably about 5-20 mole percent, based on 1 ,4- cyclohexanedicarboxylic acid ester.
• One effect of option II appears to be to convert the transesterification reaction from a simple one-step process to one more closely resembling the two-step process characteristic of the production of such polyesters as poly(1 ,4- butylene terephthalate).
• the aliphatic diol apparently participates actively, to form an aliphatic diol-terminated oligomer which, in later stages, polycondenses with elimination of the more volatile diol to form high molecular weight poly(1 ,4-cyclohexanedicarboxylate).
• C 2 - 6 aliphatic diol Although the major portion of the C 2 - 6 aliphatic diol is eliminated from the reaction mixture, it is often found that a small portion of the C 2 . 6 aliphatic diol remains in the final polymer product. Thus, when option II is employed, often about 0.5-5 mole % of the diol-derived units in the poly(1 ,4- cyclohexanedicarboxylate) may be derived from C 2 . 6 aliphatic diol and the remaining 95-99.5 mole % of the diol-derived units are derived from the relatively non-volatile diol or mixture of relatively non-volatile diols. The final proportion of C 2 .
• 6 aliphatic diol-derived units in the polymer product will be dependent upon the actual process conditions among other factors.
• option II it is also within the bounds of the present invention to prepare a poly(1 ,4-cyclohexane-dicarboxylate) with diol-derived units consisting essentially of relatively non-volatile diol or mixture of relatively non-volatile diols.
• option II it is also within the bounds of the present invention to prepare a poly(1 ,4-cyclohexanedi-carboxylate) with diol-derived units consisting of relatively non-volatile diol or mixture of relatively nonvolatile diols.
• Mw values were determined by gel permeation chromatography. Differential scanning calorimetry (DSC) values for Tm and Tc were determined on polymer samples using information from the second heat.
• DMCD and CHDM Various proportions of DMCD and CHDM (each present in about 1 mole quantity) were weighed into a glass tube reactor which was placed in a melt polymerization apparatus equipped with a stirrer, temperature programmer, temperature sensing means, vacuum controller and torque meter. The pressure was reduced to 500 torr, the mixtures were heated to 160°C in a sand bath and portions of tetraisopropyl titanate catalyst were added. Programmed heating, with stirring at 150 rpm, was then initiated as follows:
• the product of each example was a polyester with a desirably high molecular weight.
• the products had desirably high molecular weights.

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• Polyesters Or Polycarbonates (AREA)

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• 1999
  • 1999-03-30 US US09/281,529 patent/US6084055A/en not_active Expired - Lifetime
• 2000
  • 2000-02-28 JP JP2000608674A patent/JP2002540269A/ja not_active Withdrawn
  • 2000-02-28 EP EP05015514A patent/EP1598385A1/en not_active Withdrawn
  • 2000-02-28 WO PCT/US2000/005064 patent/WO2000058382A2/en not_active Ceased
  • 2000-02-28 EP EP00913647A patent/EP1175455B1/en not_active Expired - Lifetime
  • 2000-02-28 ES ES00913647T patent/ES2248058T3/es not_active Expired - Lifetime
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