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US5057261A Expired / Lapsed US ⏱️ 0.0 years remaining

Process for producing modified ultrahigh-molecular-weight polyolefins

Assignee: Mitsui Chemicals Inc
•
Filing: 1989-11-06
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Granted: 1991-10-15
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Expires: 2009-11-06
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Abstract

Abstract A process for producing a modified ultrahigh-molecular-weight polyolefin composition, which comprises mixing a powder of an ultrahigh-molecular-weight polyolefin (A) having an intrinsic viscosity of at least 5 dl/g, a flowability improver (B) having a melting point lower than the melting point of the ultrahigh-molecular-weight polyolefin (A), a monomer (C) having an olefinically unsaturated bond and a radical initiator (D) with stirring at the melting point of the flowability improver (B) or a higher temperature but below the melting point of the ultrahigh-molecular-weight polyolefin (A), and then melt-kneading them at the melting point of the ultrahigh-molecular-weight polyolefin (A) or a higher temperature to react the monomer (C) with the ultrahigh-molecular-weight polyolefin (A).

Inventors

  • 👤 Yoshiji Ohori
  • 👤 Hirofumi Harazoe

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-08 13:25
CPC Classifications
C; C08; C08F; C08F2/00; C08F2/02; C08F255/00

Claims Analysis

Total Claims: 3
Claim 1
Independent Claim 265 words
A process for producing a stretched molded article of a graft-modified ultrahigh-molecular-weight polyolefin composition, which comprises mixing 5 to 80% by weight of a powder having a particle diameter of 1 to 500 μm of an ultrahigh-molecular-weight polyolefin having an intrinsic viscosity [η] of 5 to 30 dl/g, 20 to 95% by weight of a normally solid flowability improver (B) having a melting point 20°-70° C. lower than the melting point of the ultrahigh-molecular-weight polyolefin (A), 0.1 to 20 parts by weight, per 100 parts by weight of the ultrahigh-molecular-weight polyolefin (A), of a monomer (C) selected from the group consisting of ethylenically unsaturated carboxylic acids, derivatives of the carboxylic acids, ethylenically unsaturated epoxy monomers and ethylenically unsaturated silane monomer, and 0.01 to 5 parts by weight, per 100 parts by weight of the ultrahigh-molecular-weight polyolefin (A), of a radical initiator (D) at the melting point of the flowability improver (B) or a higher temperature but below the melting point of the ultrahigh-molecular-weight polyolefin (A) to form a dispersion in which the flowability improver (B) forms the dispersion medium and the ultrahigh-molecular-weight polyolefin (A) forms the disperse phase, the monomer (C) and the radical initiator (D) exist dissolved or uniformly dispersed in the dispersion medium, and the ultrahigh-molecular-weight polyolefin (A) exists swollen with the flowability improver (B); melt-kneading the dispersion at the melting point of the ultrahigh-molecular-weight polyolefin (A) or a higher temperature; extruding the melt-kneaded mixture through a die to form an extruded article; stretching the extruded article; and removing the flowability improver (B) from the molded article before, during or after the stretching.
Claim 2
Dependent Claim 265 words
A process for producing a stretched molded article of a graft-modified ultrahigh-molecular-weight polyolefin composition, which comprises mixing 5 to 80% by weight of a powder having a particle diameter of 1 to 500 μm of an ultrahigh-molecular-weight polyolefin having an intrinsic viscosity [η] of 5 to 30 dl/g, 20 to 95% by weight of a normally solid flowability improver (B) having a melting point 20°-70° C. lower than the melting point of the ultrahigh-molecular-weight polyolefin (A), 0.1 to 20 parts by weight, per 100 parts by weight of the ultrahigh-molecular-weight polyolefin (A), of a monomer (C) selected from the group consisting of ethylenically unsaturated carboxylic acids, derivatives of the carboxylic acids, ethylenically unsaturated epoxy monomers and ethylenically unsaturated silane monomer, and 0.01 to 5 parts by weight, per 100 parts by weight of the ultrahigh-molecular-weight polyolefin (A), of a radical initiator (D) at the melting point of the flowability improver (B) or a higher temperature but below the melting point of the ultrahigh-molecular-weight polyolefin (A) to form a dispersion in which the flowability improver (B) forms the dispersion medium and the ultrahigh-molecular-weight polyolefin (A) forms the disperse phase, the monomer (C) and the radical initiator (D) exist dissolved or uniformly dispersed in the dispersion medium, and the ultrahigh-molecular-weight polyolefin (A) exists swollen with the flowability improver (B); melt-kneading the dispersion at the melting point of the ultrahigh-molecular-weight polyolefin (A) or a higher temperature; extruding the melt-kneaded mixture through a die to form an extruded article; stretching the extruded article; and removing the flowability improver (B) from the molded article before, during or after the stretching.
Claim 3
Dependent Claim 41 words
The process of claim 1 in which the monomer (C) is an ethylenically unsaturated silane monomer; and the silane monomer is crosslinked by impregnating the stretched molded article with a silane crosslinking catalyst and then contacting the molded article with moisture.

References Cited (Backward Citations)

JPS6157604A Cited
EP0173572B1 Cited
EP0229477A2 Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1994-10-14 1995-04-15 1995-10-15 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1998-10-14 1999-04-15 1999-10-15 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2002-10-14 2003-04-15 2003-10-15 $7700.00 Window Closed / Lapsed

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