US 4,880,856 AGrant
Enhancing Color Stability of Sterilizing Radiation of Polymer Compositions
Issue Date:1989-11-14
•14 Claims
Abstract
Compounds having defined thiazole functional groups are described which color stabilize aromatic carbonate polymers or blends therewith upon exposure to sterilizing radiation.
Metadata
Assignee
- General Electric Company
Inventor
- Roger W. Avakian
Application Information
Application Number:US 1366025
Filing Date:1987-12-22
Priority Date:1987-12-22
Art Unit:153
Classifications
IPC:
C08K 534
Field of Search:
522524523163;51;7583136
Patent Drawings
This patent does not have any drawings.
Description
DESCRIPTION OF SPECIFIC EMBODIMENTS
Further illustration of this invention is set forth in the following examples. There is no intention to limit the scope of the invention to merely what is shown.
The following resins were used in the formulations of the examples:
Polycarbonate--LEXAN.RTM. 145 resin, poly(bisphenol-A carbonate), General Electric Company (contains 0.06% by weight of a conventional phosphite stabilizer).
Poly(ester-carbonate)--an ester content of 75% mole % and being 93 mole % isophthalate and 7 mole % terephthalate.
Polycarbonate/polyester blend--80 weight parts polycarbonate with 20 weight parts KODAR A150 resin, Eastman Kodak Company, poly(1,4-cyclohexanedimethanol-terephthalate-co-isophthalate) and a phosphorous acid stabilizer.
Unless otherwise noted, the formulations containing 100 weight parts of the indicated resin or blend were extruded on a sterling single screw (13/4') extruder at a melt temperature of T1. Test plaques 1/8' in thickness were injection molded on a 3 oz. Van Dorn using a T2 melt set temperature, a T3 mold cavity temperature, and a 10/20 cycle time. T1, T2, and T3 were set according to the resin or blend used:
The samples were irradiated by one of the following methods:
Gamma Irradiation--samples were exposed to a Co.sup.60 source on a continuous conveyor system, dosimetry was monitored with a calibrated NBS, radiochromic, nylon dosimeter and different Co.sup.60 sources were used.
Electron Beam Irradiation--samples irradiated on one side in air using a linear cathode electron beam system, 5 Mrad dose, 20 ft/min line speed, 5 mA beam current, 200 KV terminal voltage, dosimetry monitored with a calibrated NBS, radiochromic, nylon dosimeter.
Unless otherwise noted, testing of the samples has been conducted with gamma radiation and yellowness index, Y.I., measured on a Gardner colorimeter in accordance with ASTM D1925 both before and after radiation. The less change in Y.I. upon irradiation, the more effective the stabilizer.
EXAMPLES 107-118
The following formulations were extruded at from 271.degree. to 299.degree. C. and injection molded into test plaques 1/8' in thickness using a melt temperature of from 271.degree. to 288.degree. C. and a mold temperature of from 49.degree. to 82.degree. C. Measurement of yellowness index was made on a Pacific-Scientific Spectrogard II unit in accordance with ASTM D1925.
EXAMPLE 121
The following composition was extruded from 260.degree. to 316.degree. C. and injection molded into test plaques 1/8' in thickness using a melt temperature of from 260.degree. to 304.degree. C. Measurement of yellowness index was made on a Pacific Scientific Spectrogard II unit in accordance with ASTM D-1925.
EXAMPLES 129-131
The following formulations were molded in accordance with the conditions of Examples 107-118:
Claims
What is claimed is:
1. A composition comprising an aromatic carbonate polymer in admixture with an effective amount of thiol stabilizing compound effective to inhibit yellowing upon exposure to sterilizing radiation, wherein said thiol stabilizing compound is 2.5-dimercapto-1,3,4-thiadiazole.
2. The composition of claim 1 wherein said aromatic carbonate polymer is a poly(bisphenol-A) carbonate.
3. The composition of claim 1 wherein said aromatic carbonate polymer is a poly(ester-carbonate).
4. The composition of claim 1 which further comprises a polyester resin.
5. A composition comprising an aromatic carbonate polymer in admixture with an amount of a thiol stabilizing compound effective to inhibit yellowing upon exposure to sterilizing radiation, wherein said thiol is 2-mercaptobenzothiazole.
6. The composition of claim 1 which contains 0.01-5.0 weight parts stabilizing compound per 100 weight parts polymer.
7. The combination of claim 1 which contains 0.01-0.50 weight parts stabilizing compound per 100 weight parts polymer.
8. The composition of claim 1 which further comprises a polyestercarbonate resin.
9. The composition of claim 5 wherein said aromatic carbonate polymer is a poly(bisphenol-A) carbonate.
10. The composition of claim 5 wherein said aromatic carbonate polymer is a poly(ester-carbonate).
11. The composition of claim 5 which further comprises a polyester chain.
12. The composition of claim 5 which contains 0.01-5.0 weight parts stabilizing compound per 100 weight parts polymer.
13. The composition of claim 5 which contains 0.01-0.50 weight parts stabilizing compound per 100 weight parts polymer.
14. The composition of claim 5 which further comprises a polyestercarbonate resin.
Patent Citations (41)
| Patent | Date | Inventor | Cited By |
|---|---|---|---|
| US2288282 | 1942-06-01 | Huismann | |
| US2465319 | 1949-03-01 | Rex et al. | |
| US2739171 | 1956-03-01 | Linn | |
| US2901466 | 1959-08-01 | Kibler et al. | |
| US2960453 | 1960-11-01 | Cook et al. | |
| US2999835 | 1961-09-01 | Goldberg | |
| US3028365 | 1962-04-01 | Schnell et al. | |
| US3030331 | 1962-04-01 | Goldberg | |
| US3047539 | 1962-07-01 | Pengilly | |
| US3112291 | 1963-11-01 | Anderson | |
| US3148172 | 1964-09-01 | Fox | |
| US3153008 | 1964-10-01 | Fox | |
| US3169121 | 1965-02-01 | Goldberg | |
| US3175992 | 1965-03-01 | Anderson | |
| US3207814 | 1965-09-01 | Goldberg | |
| US3247160 | 1966-04-01 | Anderson | |
| US3251807 | 1966-05-01 | Deanin et al. | |
| US3254047 | 1966-05-01 | Caldwell et al. | |
| US3264264 | 1966-08-01 | Baker | |
| US3334154 | 1967-08-01 | Kim | |
| US3386935 | 1968-06-01 | Jackson et al. | |
| US3475372 | 1969-10-01 | Gable | |
| US3475373 | 1969-10-01 | Jackson et al. | |
| US3494885 | 1970-02-01 | Thompson et al. | |
| US3535300 | 1970-10-01 | Gable | |
| US3537967 | 1970-11-01 | Kelley et al. | |
| US3622538 | 1971-11-01 | Green | |
| US3940325 | 1976-02-01 | Hirao | |
| US4001184 | 1977-01-01 | Scott | |
| US4018750 | 1977-04-01 | Onizawa | |
| US4123436 | 1978-10-01 | Holub et al. | |
| US4131575 | 1978-12-01 | Adelmann et al. | |
| US4156069 | 1979-05-01 | Prevorsek et al. | |
| US4162354 | 1979-07-01 | Pearson et al. | |
| US4194038 | 1980-03-01 | Baker et al. | |
| US4303759 | 1981-12-01 | Dixon et al. | |
| US4431497 | 1984-02-01 | Rekers | |
| US4686245 | 1987-08-01 | Nelson | |
| EPX162012 | 1985-11-01 | ||
| JPX44-2480 | 1969-02-01 | ||
| JPX5084352 | 1980-06-01 |