US 3,998,908 AGrant
Process for the Manufacture of Stabilized Polyester-Polycarbonate Copolymers
Issue Date:1976-12-21
•17 Claims
Abstract
The melt phase reaction and/or solid phase reaction for the manufacture of polyesters is accelerated by adding a polycarbonate and a phosphorus containing stabilizer to the reaction mixture before completion of the reaction.
Metadata
Assignee
- Ciba-Geigy Corporation
Inventor
- Lothar Buxbaum
Application Information
Application Number:US 5246881
Filing Date:1974-11-18
Priority Date:1973-11-23
Art Unit:141
Classifications
IPC:
C08G 6364
Field of Search:
260860;45.7 P
Patent Drawings
This patent does not have any drawings.
Description
The examples which follow explain the invention in more detail.
The relative viscosity is determined on solutions of 1 g of polyester in 100 ml of a mixture consisting of equal parts of phenol and tetrachloroethane, at 30.degree. C. The carboxyl end group concentration is determined after dissolving the sample in pure anhydrous benzyl alcohol and subsequent dilution with chloroform, by titration with 0.02 N sodium hydroxide solution in benzyl alcohol, against Phenol Red. The values are quoted in equivalents per 10.sup.6 g and can be calculated from the formula ##EQU1##
EXAMPLE 1:
3,000 g of dimethyl terephthalate (DMT), 2,480 g of ethylene glycol, 1.31 g of zinc acetate and 1.4 g of antimony trioxide are filled into a 10 liter reactor equipped with a stirrer, nitrogen inlet, condenser and temperature measuring device, and the mixture is heated to 145.degree. C. 99% of the amount of methanol to be expected theoretically are distilled off over the course of 4 hours whilst stirring and passing nitrogen through the apparatus, during which time the temperature of the reaction mixture rises to 210.degree. C.
The reaction mixture is then transferred into a second reactor and heated to 240.degree. C. A vacuum of 50 mm Hg is then applied over the course of half an hour by means of a water pump and at the same time the reaction temperature is raised to 275.degree. C. Whilst keeping the reaction temperature constant, the vacuum is improved, by means of a vacuum pump, to 0.7 mm Hg over the course of half an hour and is kept thereat for a further 1.5 hours. A sample withdrawn at that time, after releasing the vacuum by means of nitrogen, shows a relative viscosity of 1.6. 0.8% by weight of bisphenol A polycarbonate of relative viscosity 1.68 is added and a vacuum of 0.7 mm Hg is immediately applied again. The relative viscosity rose to 1.92 over the course of 10 minutes. The melt is extruded through dies to give ribbons and the ribbons are chilled in water and comminuted to give cylindrical granules of 2 .times. 3 mm.
300 g of these granules are first dried, and crystallised, for 2 hours under a vacuum of 0.3 mm Hg at 140.degree. C in a 1 liter Rotavapor flask dipping into an oil bath, and the reaction is then continued for 6 hours in the solid phase at 235.degree. C under the same vacuum. The end product has a relative viscosity of 2.76.
EXAMPLE 2 (comparison example)
Polyethylene terephthalate without added polycarbonate was manufactured analogously to Example 1. In this case it required 1 hour to pass from a relative viscosity of 1.60 to 1.92. This material was also converted to granules and the reaction was continued in the solid phase in the Rotavapor flask. The relative viscosity was 2.44 after 6 hours at 235.degree. C.
EXAMPLE 3 (comparison example)
The procedure followed was analogous to Example 1 but instead of the polycarbonate 0.8% by weight of diphenyl carbonate was added.
Hereupon, the vacuum fell to 120 mm Hg since the diphenyl carbonate partially evaporated. It was also not possible to improve the vacuum since the vacuum pipeline was clogged by diphenyl carbonate and by reaction mixture which foamed over. Hence, the reaction had to be discontinued 15 minutes after adding the diphenyl carbonate. During this time, the relative viscosity rose from 1.60 to 1.78.
EXAMPLE 4
2,910 g of dimethyl terephthalate (DMT), 1,860 g of ethylene glycol, 534 g of 1,1-methylene-bis-[3-(2'-hydroxyethyl)-5,5-dimethylhydantoin] (M-DHM) (10 mol % based on DMT), 0.99 g of zinc acetate and 1.05 g of antimony trioxide are introduced into a 10 liter reactor equipped with a stirrer, nitrogen inlet, condenser and temperature measuring device and the mixture is heated to 150.degree. C. 98% of the amount of methanol to be expected theoretically are distilled off over the course of 3.5 hours whilst stirring and passing nitrogen through the apparatus; during this time the temperature of the reaction mixture rises to 200.degree. C.
The reaction mixture is then heated to 240.degree. C and a vacuum of 50 mm Hg is applied over the course of half an hour by means of a water pump and at the same time the reaction temperature is raised to 265.degree. C. Whilst keeping the reaction temperature the same, the vacuum is improved to 0.7 mm Hg over the course of half an hour, by means of a vacuum pump, and is maintained for a further 2.5 hours. A sample withdrawn at this time by releasing the vacuum with nitrogen shows a relative viscosity of 1.60. 1.5% by weight of 2,2-(4,4'-dihydroxydiphenyl)-propane polycarbonate of relative viscosity 1.68 are added and a vacuum of 0.7 mm Hg is immediately applied again. The relative viscosity rose to 1.86 over the course of 8 minutes.
The melt is extruded through nozzles to produce ribbons which are chilled in water and comminuted to colourless cylindrical granules of size 2 .times. 3 mm.
300 g of these granules are pre-crystallised in acetone, and are then first dried for 1 hour under a vacuum of 0.3 mm Hg at 80.degree. C and next heated to 210.degree. C over the course of 6 hours, both operations being carried out in a 1 liter Rotavapor flask dipping into an oil bath. After a further 18 hours at this temperature, the relative viscosity of the granules had risen to 2.44.
EXAMPLE 5 (comparison example)
A copolyester is prepared analogously to Example 4, but without addition of the polycarbonate. After 4.5 hours reaction time at 265.degree. C, a relative viscosity of 1.84 was reached. The colour of the granules was yellow.
During the subsequent solid phase reaction a relative viscosity of only 2.14 was achieved over the course of 96 hours.
EXAMPLES 6-22
Low molecular polyesters of a certain relative viscosity are manufactured, the reaction being carried out analogously to Examples 1 and 4. A certain amount of 2,2-(4,4'-dihydroxyphenyl)-propane polycarbonate of relative viscosity 1.68 is then added and after applying a vacuum, the reaction is continued in the melt phase. The composition of the polyesters and of the catalyst used to manufacture the precondensate, the reaction times and the characteristic data of the end products can be seen from Table 1.
After spinning and granulation, the condensates from Examples 18-22 were condensed further for 17 hours (only 16 hours in the case of Example 19) in the solid phase, the temperature being 230.degree. C and the pressure 0.2 mm Hg. The relative viscosities were 1.97 (Example 18), 2.14 (Example 19), 2.18 (Example 20), 2.26 (Example 21) and 2.43 (Example 22).
EXAMPLES 23-27
A low molecular polyester having the relative viscosity indicated in Table 2 is manufactured analogously to Example 1. Thereafter, a certain amount (see Table 2) of 2,2-(4,4'-dihydroxyphenyl)-propane polycarbonate and a certain amount (see Table 2) of stabiliser are added and after application of a vacuum the reaction is continued in the melt phase. The viscosity, reaction time and colour can be seen from Table 2.
Comparison examples 28 and 29
3,000 g of dimethyl terephthalate, 2,800 g of 1,4-butanediol and 1.78 g of titanium tetraisopropylate are introduced, analogously to Examples 25-26, into a 10 l reactor equipped with a stirrer, nitrogen inlet and separating column. 99% of the theoretical amount of methanol are distilled off over the course of 4.5 hours whilst stirring and passing nitrogen through the reactor, during which time the temperature of the reaction mixture rises to 200.degree. C.
The mixture is then transferred into a second reactor, a vacuum of 0.5 mm Hg is applied over the course of 1.5 hours and at the same time the reaction temperature is raised to 250.degree. C. After 0.5 mm Hg was reached for the first time, 1% by weight of ODP is added in one case and 1% by weight of tris-nonylphenyl phosphite is added in the other case. A vacuum is then applied again and the polycondensation reaction is continued. In both cases, however, no molecular weight increase occurs. The melt remains very mobile.
EXAMPLE 30
3,000 g of dimethyl terephthalate, 2,783 g of 1,4-butanediol, 1.01 g of zinc acetate and 0.63 g of dibutyl-tin oxide are introduced into a 10 l reactor equipped with a stirrer, nitrogen inlet, condenser and temperature-measuring device and the mixture is heated to 150.degree. C. 98% of the amount of methanol to be expected theoretically, together with some tetrahydrofurane formed, are distilled off over the course of 4 hours whilst stirring and passing nitrogen through the reactor, during which time the temperature of the reaction mixture rises to 215.degree. C.
The reaction mixture is then transferred into a second reactor and heated to 244.degree. C. A vacuum of 70 mm Hg is then applied over the course of half an hour by means of a water pump and at the same time the reaction temperature is raised to 255.degree. C. The vacuum is then improved to 0.7 mm Hg over the course of half an hour whilst adjusting the reaction temperature to 250.degree. C, and is maintained for a further 45 minutes. At this time, the relative viscosity corresponds to 1.80. 60 g of a bisphenol A polycarbonate of relative viscosity 1.68 are then added under vacuum, using a vacuum lock. The current taken by the stirrer rose so greatly over the course of 7 minutes that the reaction had to be discontinued. After spinning the melt through nozzles, and granulating the product, a relative viscosity of 2.48 is measured.
300 g of these granules are heated to 210.degree. C under a vacuum of 0.3 mm Hg in a 1 liter Rotavapor flask dipping into an oil bath, and are left at this temperature for 5 hours. The end product from this solid phase condensation has a relative viscosity of 3.05.
EXAMPLE 31 (comparison example)
The procedure followed is exactly as in Example 30 but without addition of bisphenol A polycarbonate. 67 minutes are required to pass from a relative viscosity of 1.8 to a relative viscosity of 2.39.
Claims
What we claim is:
1. An improved process for the manufacture of thermoplastic polyesters containing carbonate groups and a stabilizer containing phosphorus from linear polyester precondensates which still contain hydroxyl groups, characterized in that linear polyesters containing hydroxyl groups and having a relative viscosity of at least 1.30, measured at 30.degree. C on a 1% strength solution in equal parts of phenol and tetrachloroethane, are allowed to react with 0.01 to 45% by weight, based on the total amount, of a polycarbonate built up from diols of which the hydroxyl groups are bonded to one or different aromatic radicals and which polycarbonate has a degree of polycondensation of at least 10, in the melt phase or solid phase, at a temperature of 170.degree. to 320.degree. C and in vacuo, in a stream of inert gas, or in vacuo and a stream of inert gas wherein the improvement comprises increasing the relative viscosity of said thermoplastic polyesters by adding 1 to 15% by weight, based on the polyester precondensate, of a stabilizer containing phosphorus simultaneously with the addition of the polycarbonate.
2. A process according to claim 1, characterised in that a polyester precondensate is employed which contains at least 80 mol % of terephthalic acid radicals and at least 80 mol % of radicals of an aliphatic diol with 2 to 10 carbon atoms or of 1,4-dihydroxymethylcyclohexane.
3. A process according to claim 2, characterised in that the aliphatic diol contains 2 to 4 carbon atoms.
4. A process according to claim 2, characterised in that the polyester precondensate is built up from terephthalic acid and linear alkylenediols with 2 to 4 carbon atoms.
5. A process according to claim 1, characterised in that the polyester precondensate contains co-condensed diol radicals which possess secondary or phenolic alcohol groups.
6. A process according to claim 1, characterised in that the polyester precondensate contains at least 50% of hydroxyl end groups, based on the total end groups present.
7. A process according to claim 1, characterised in that the polyester precondensate has a relative viscosity of 1.5 to 3.5.
8. A process according to claim 7, characterised in that the polyester precondensate has a relative viscosity of 1.6 to 2.5.
9. A process according to claim 1, characterised in that 2,2-(4,4'-dihydroxydiphenyl)-propane polycarbonate is used as the polycarbonate.
10. A process according to claim 1, characterised in that the degree of polycondensation of the polycarbonate is at least 100.
11. A process according to claim 1, characterised in that 0.01 to 30% by weight of a polycarbonate are added.
12. A process according to claim 11, characterised in that 0.1 to 20% by weight of a polycarbonate are added.
13. A process according to claim 12, characterised in that 0.1 to 3% by weight of a polycarbonate are added.
14. A process according to claim 1, characterised in that the reaction in the melt phase is carried out continuously in an extruder.
15. A process according to claim 1, characterised in that polyester scrap is employed as the polyester precondensate.
16. A process according to claim 1 wherein the stabilizer containing phosphorus is a triaryl phosphate or triaryl phosphite.
17. A process according to claim 1 wherein the stabilizer containing phosphorus is selected from the group consisting of triphenyl phosphate, tris-nonylphenyl phosphate, triphenyl phosphite and bis(n-octadecyl) 3,5-di-tert-butyl-4-hydroxybenzylphosphonate.
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