Application of William C. Rainer, Edward M. Redding, Joseph J. Hitov, Arthur W. Sloan and William D. Stewart

377 F.2d 1006, 54 C.C.P.A. 1445, 153 U.S.P.Q. (BNA) 802, 1967 CCPA LEXIS 300
CourtCourt of Customs and Patent Appeals
DecidedJune 2, 1967
DocketPatent Appeal 7668
StatusPublished
Cited by6 cases

This text of 377 F.2d 1006 (Application of William C. Rainer, Edward M. Redding, Joseph J. Hitov, Arthur W. Sloan and William D. Stewart) is published on Counsel Stack Legal Research, covering Court of Customs and Patent Appeals primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Application of William C. Rainer, Edward M. Redding, Joseph J. Hitov, Arthur W. Sloan and William D. Stewart, 377 F.2d 1006, 54 C.C.P.A. 1445, 153 U.S.P.Q. (BNA) 802, 1967 CCPA LEXIS 300 (ccpa 1967).

Opinion

RICH, Judge.

The appeal is from decisions of the Board of Appeals, 1 affirming the examiner’s rejection of claims 2-6, 8-12, 17, 20, and 48-59 in application serial No. 12,339, filed March 2, 1960, entitled “Polyethylene.” Claims 18 and 63 have been allowed.

Introduction

The invention relates to graft copolymers of polyethylene and certain other *1008 compounds, their method of preparation, and articles made thereof. The following claims are typical of those rejected:

2. A process comprising irradiating normally solid polyethylene at a dosage of at least about 2 X 10° REP in contact with a material selected from the group consisting of a polymerizable ethylenically unsaturated hydrocarbon monomer other than ethylene, halogenated styrene, alkyl acrylates, alkyl methacrylates, dialkenyl oxalates, diallyl phthalate, diallyl maléate, diallyl fumarate, dialkyl maleates and dialkyl fumarates to form a graft polymer.
9. A bottle made of irradiated polyethylene, the irradiation being to an extent of at least 2 X 10° REP, having grafted thereto a polymer formed by polymerizing a member of the group consisting of a polymerizable ethylenically unsaturated hydrocarbon monomer other than ethylene, halogenat■ed styrene, alkyl acrylates, alkyl methacrylates, N,N-methylene-bis-acrylamide, dialkenyl oxalates, diallyl phthalate, triallyl cyanurate, diallyl maleate, diallyl fumarate, triallyl melamine, dialkyl maleates and dialkyl fumarates on said polyethylene.
17. A graft polymer of irradiated polyethylene with a polymer of an ethylenically unsaturated hydrocarbon monomer, other than ethylene, said polymer of said monomer being formed in the presence of said polyethylene, said irradiation being to an extent of at least 2 X 10° REP.
49. The process of preparing a shaped article exhibiting dimensional and thermal stability and resistance to oxidative degradation at temperatures up to 250 °C. which comprises (1) preparing an intimate mixture of from 60 to 95 parts by weight of (a) polyethylene, and a complementary proportion of from 40 .to 5 parts by weight of (b) at least one organic compound selected from the group consisting of monomeric esters of methacrylic acid and monomeric esters of acrylic acid; (2) preparing a shaped article from said mixture, and (3) irradiating said shaped article with high energy, ionizing radiation for a time sufficient to provide a radiation dose of from 36 X 10“ rads to 720 X 10“ rads.
57. A bottle made of irradiated polyethylene, the irradiation being "to an extent of at least 2 X 10° REP, having grafted thereto a polymer formed by polymerizing a material selected from the group consisting of a polymerizable ethylenically unsaturated hydrocarbon monomer other than ethylene, alkyl acrylates and alkyl methacrylates.

Claims 3-6, and 12, 20, and 48 are dependent upon claim 2 and recite additional limitations including the presence of a “free radical engendering compound,” an inert atmosphere, a vacuum, an irradiation dosage of at least 6 X 10“ REP 2 and a temperature of at least the transition point of polyethylene. Claim 8 restricts the material in contact with polyethylene in the process of claim 2 to a hydrocarbon monomer.

Claims 10 and 11 restrict the polymer coating of claim 9 to the exterior and interior of the bottle respectively.

Claims 50-54 and 56 are process claims which require the same three basic steps as claim 49. Claim 55 is directed to a shaped article made by the process of claim 49.

Claims 58 and 59 restrict the polymer coating of claim 57 to the exterior and interior of the bottle respectively.

The board affirmed rejections of the appealed claims on the bases of res judicata, obviousness, inadequate disclosure, and indefiniteness (improper Markush group). It relied on In re Rainer, 305 F.2d 505, 49 CCPA 1243 (1962), Lawton *1009 et al, Irradiation of Polymers by High-Energy Electrons, 172 Nature 76-77 (1953) and the following patents:

Cole 2,919,473 January 5, 1960 Brophy 2,670,483 March 2, 1954

In In re Rainer, while reversing as to some claims, we affirmed rejections of several claims in an application of which the present application is a continuation-in-part. The former application was concerned with “condensation products of polyethylene with other polymers and ethylenieally unsaturated monomers,” characterized as “new cross linked polymers of increased strength and rigidity * * *.” These were prepared by the irradiation of polyethylene “in the presence of other non-polar or only slightly polar polymers or ethylenieally unsaturated monomers.” The following claims are typical of those whose rejection was affirmed:

31. A process comprising irradiating normally solid polyethylene at a dosage of at least about 2 X 10° REP admixed with a material selected from the group consisting of hydrocarbon polymers containing a plurality of isobutylene units, a liquid partially depolymerized rubber, a liquid butadiene styrene copolymer, a liquid butadiene acrylonitrile polymer, a polymerizable ethylenieally unsaturated hydrocarbon monomer other than ethylene, halogenated styrene, alkyl acrylates, alkyl methacrylates, N.N-methylene-bis-acrylamide, dialkenyl oxalates, diallyl phthalate, ethylene glycol dimethacrylate, triallyl cyanurate, diallyl maleate, diallyl fumarate, triallyl melamine, dialkyl maleates and dialkyl fumarates to form a cross-linked polyethylene copolymer.
39. A process comprising irradiating normally solid polyethylene at a dosage of between about 2 X 106 REP and 200 X 10° [REP] with high energy radiation equivalent to at least about 750,000 electron volts admixed with a material selected from the group consisting of hydrocarbon polymers containing a plurality of isobutylene units, a liquid partially depolymerized rubber, a liquid butadiene styrene copolymer, a liquid butadiene acrylonitrile polymer, a polymerizable ethylenieally unsaturated hydrocarbon monomer other than ethylene, halogenated styrene, alkyl acrylates, alkyl methacrylates, N,N-methylene-bis-acrylamide, dialkenyl oxalates, diallyl phthalate, ethylene glycol dimethacrylate, triallyl cyanurate, diallyl maleate, diallyl fumarate, triallyl melamine, dialkyl maleates and dialkyl fumarates to form a cross-linked polyethylene co-polymer.
40. A process according to claim 39 in which said material is a polymerizable .ethylenieally unsaturated hydrocarbon monomer.

The Lawton et al. (hereafter Lawton) reference describes the irradiation of various polymers and lists those which became cross-linked and those which became degraded. The former include:

Polyacrylic esters Polystyrene Polyesters Nylon Polyethylene Chlorinated polyethylene Chlorosulphonated polyethylene Natural rubber GRS Butadiene-acrylonitrile copolymers Neoprene-W Neoprene-GN Polydimethylsiloxanes Styrene-acrylonitrile copolymers

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377 F.2d 1006, 54 C.C.P.A. 1445, 153 U.S.P.Q. (BNA) 802, 1967 CCPA LEXIS 300, Counsel Stack Legal Research, https://law.counselstack.com/opinion/application-of-william-c-rainer-edward-m-redding-joseph-j-hitov-ccpa-1967.