US2008061468A1PendingUtilityA1
Fiber processing of high ethylene level propylene-ethylene random copolymers by use of nucleators
Est. expirySep 7, 2026(~0.1 yrs left)· nominal 20-yr term from priority
D01F 6/30D01F 1/10
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Claims
Abstract
A method of processing a high ethylene random copolymer comprising nucleating a high ethylene random copolymer to form a high ethylene polymeric composition, melting and extruding a high ethylene polymeric composition, spinning a high ethylene polymeric composition to form a fiber, cooling the fiber, guiding the fiber with an aspirator, and recovering the fiber.
Claims
exact text as granted — not AI-modified1 . A method of processing a high ethylene random copolymer comprising:
nucleating a high ethylene random copolymer to form a high ethylene polymeric composition, melting and extruding a high ethylene polymeric composition, spinning a high ethylene polymeric composition to form a fiber, cooling the fiber, guiding the fiber with an aspirator, and recovering the fiber.
2 . The method of claim 1 further comprising partially or fully orienting the fiber.
3 . The method of claim 1 wherein the aspirator comprises an aspirator wand.
4 . The method of claim 1 wherein the fiber is recovered by winding the fiber on spools.
5 . The method of claim 1 wherein the high ethylene random copolymer has an ethylene content greater than 3 wt. %.
6 . The method of claim 1 wherein the high ethylene random copolymer has a xylene solubles content greater than 5 wt. % as measured in accordance with ASTM D 5492-98.
7 . The method of claim 1 wherein the high ethylene polymeric composition further comprises a visbreaker in amounts ranging from 50 ppm to 1000 ppm.
8 . The method of claim 1 wherein the high ethylene random copolymer comprises an ethylene-propylene random copolymer.
9 . The method of claim 1 wherein the high ethylene random copolymer comprises a copolymer of ethylene and an alpha olefin monomer.
10 . The method of claim 1 wherein the high ethylene random copolymer has a melt flow rate of from 1 g/10 min to 1,000 g/10 min, as determined in accordance with ASTM D-1238.
11 . The method of claim 1 wherein the high ethylene random copolymer has a melting point of less than 140° C.
12 . The method of claim 1 wherein the nucleating agent comprises a norbornane carboxylic acid salt in amounts from 50 ppm to 1000 ppm.
13 . The method of claim 1 wherein the nucleating agent comprises an organophosphate, a sodium benzoate, metal benzoate, a sorbitol compound, a sorbitol derivative, dibenzylidene sorbitol, talc, or combinations thereof.
14 . The method of claim 13 wherein the nucleating agent is present in amounts from 50 ppm to 3000 ppm.
15 . The method of claim 1 wherein the high ethylene polymeric composition has an initial tensile modulus of from 60,000 psi to 90,000 psi, as measured in accordance with ASTM D-638.
16 . The method of claim 1 wherein the high ethylene polymeric composition has an initial stiffness as measured by the flexural modulus of from 60,000 psi to 90,000 psi, as measured in accordance with ASTM D-790.
17 . The method of claim 1 wherein the fiber has a tenacity greater than or equal to 1.0 g/den as measured in accordance with ASTM D-3822.
18 . The method of claim 1 wherein the fiber has a draw ratio of from 2.0:1 to 5.0:1.
19 . The method of claim 1 wherein the fiber has a 5% secant modulus of from 2.0 g/den to 20.0 g/den as measured in accordance with ASTM D-882.
20 . The method of claim 1 wherein the fiber has a denier per filament of from 1.0 g/9000 meters to 20.0 g/9000 meters as measured in accordance with ASTM D1907-01.Join the waitlist — get patent alerts
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