Thermoplastic polymer compositions

Synthetic resins or natural rubbers -- part of the class 520 ser – Synthetic resins – Mixing of two or more solid polymers; mixing of solid...

Reexamination Certificate

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C525S221000, C525S222000, C525S227000, C525S228000, C525S240000

Reexamination Certificate

active

06407172

ABSTRACT:

CROSS-REFERENCE TO RELATED APPLICATIONS
This application claims the benefit of priority to European Patent Application 97203986.1 dated Dec. 18, 1987 via corresponding International Application Number PTC/U98/26423 filed Dec. 11, 1998 and published as WO 99/31177 on Jun. 24, 1999.
BACKGROUND OF THE INVENTION
This invention relates to thermoplastic polymer compositions which are thermoformable, and to thermoformed articles made from such compositions.
The compositions of the present invention, which are halogen-free, are useful for making laminates, sheets and films, and for replacing polyvinyl chloride (PVC) resins in many of their traditional uses. In particular, compositions of the present invention, and thermoformed articles made therefrom, are suitable as PVC replacements in the automotive field. They may be used in the fabrication of interior sheathing of automobiles, for example, in the instrument panel skins, door panels, roof liners and seat covers.
Automotive applications require certain properties in the resins, including good flexibility, low temperature properties, capability of providing a soft surface texture and grain retention; as well as good high temperature properties and low emissions associated with it in view of the extreme temperatures the interior of automobiles can reach on hot, sunny days. PVC-free compositions comprising a blend of polypropylene, ethylene copolymer ionomer resin, ethylene/glycidyl acrylate or methacrylate copolymer, and uncrosslinked ethylene propylene rubber are described in U.S. Pat. No. 5,206,294. Such a blend has been proven suitable for most applications and it is characterized by good thermoformability and grain retention. This blend has some drawbacks, however, in applications where thin gauges are required. At gauges around 1 mm and thinner, the low embossing depth may lead to insufficient grain retention; moreover, this blend may be too costly for certain applications.
DE 196 10 415, assigned to Schulman GMBH. discloses compounds for injection molding application. The compositions include a polyolefin, a noncrosslinked cthylone propylene copolymer, an ionomeric copolymer, a carboxylic acid compound and an epoxide compound. The epoxide compound must be of the following formula:
wherein n=0-10, R
1
=hydrogen, an alkyl, aralkyl or aryl group, and R
2
is an alkyl, aralkyl, alkylalkoxy, cycloalkyl, or cycloalkenyl group, and R
3
is
if n is not equal to 0, and R
3
=hydrogen if n=0.
The epoxide compound may be n-butylglyidyl ether, 2-ethylhexylglycidyl ether, glycidyl ethers of long-chain aliphatic alcohols, among others.
EP 0 452 010 A2 discloses thermoplastic resin compositions, having good toughness and resistance to heat deformation, comprising crystalline propylene polymer, random stytenic copolymer, clastomeric olefin polymer selected from ethylene-propyleno-copolymer, ethylene-propylene-diene terpolymers, etc., and an epoxy group-containing olefinic copolymer.
SUMMARY OF THE INVENTION
The present invention provides a composition suitable for thermoforming which demonstrates good grain retention at thin gauges, low gloss and whose cost is competitive for many applications. This composition contains (a) 10-35 wt. % of polypropylene or an ethylene/propylene copolymer, (b) 0-30 wt. % uncrosslinked ethylene propyleie copolymer rubber having an ethylene content of 60-80 wt. %, (c) 10-25 wt. % of an ionomeric copolymer of ethylene and an &agr;,&bgr;-unsaturated C
3
-C
8
carboxylic acid, (d) 2-6 wt. % of a copolymer of ethylene and glycidyl acrylate or glycidyl methacrylate, (e) 5-20 wt. % polyethylene, and (f) 0-25 wt. % of an ethylene alpha-olefin copolymer elastoiner. As such the present invention also provides a thermoforned article made from the above composition and in particular a thermoformed instrument panel skih); including such articles that are laminated to foam prior to thermoforming.
DETAILED DESCRIPTION OF THE INVENTION
Component (a) of the composition may be a polypropylene or an ethylene/propylene copolymer, or a mixture thereof. Where component (a) contains a polypropylene, the polypropylene component consists of crystalline polypropylene and is intended to include in addition to the homopolymer those polymers that also contain minor amounts, usually not greater than 15 wt %, of higher or lower &agr;-olefins, e.g. those containing 3-8 carbon atoms, such as ethylene, butene, octene, etc. The polypropylene polymers useful in this invention have melt indices in the range of from about 0.07-30 g/10 min at 230° C./2.16 kg.
Where component (a) contains an ethylene/propylene copolymer, the copolymer will contain usually more than 15 wt % ethylene. Such polymers are well known to those skilled in the art and are commercially available.
Component (a) is present in the composition of the present invention in amounts of 10-35 wt. %, preferably 20-30 wt. %.
The uncrosslinked ethylene/propylene copolymer rubber (component (b)) may be an ethylene/propylene
onconjugated diene copolymer (EPDM) or an ethylene/propylene copolymer (EPM). EPDMs are preferred as component (b). The uncrosslinked ethylene/propylene copolymer rubber contains about 60-80 wt. %, usually about 65-75 wt % ethylene.
The nonconjugated dienes can contain from 6-22 carbon atoms having at least one readily polymerizable double bond. The amount of nonconjugated diene is generally from about 1-7 wt. %, usually 2-5 wt. %. EPDM copolymers that are especially preferred are ethylene/propylene/1,4-hexadiene, ethylene/propylene/dicyclopentadiene, ethylene/propylene
orbornene, ethylene/propylene/methylene-2-norbornene and ethylene/propylene/1,4-hexadiene
orbornadiene. It is preferred that the ethylene/propylene copolymer rubber are non-crosslinked. The ethylene/propylene copolymer rubber present as component (a)(ii) in the blend is present in amounts of 15-50 wt. %, preferably 15-40 wt. %.
Component (b) is present in the composition of the present invention in amounts of 0-30 wt. %, preferably 10-30 wt. %.
The ionic copolymer of ethylene and an &agr;,&bgr;-unsaturated C
3
-C
8
carboxylic acid (component (c)) optionally contains at least one softening comonomer that is copolymerizable with ethylene. Acrylic and methacrylic acids are preferred acid comonomers. The softening comonomer can be an alkyl acrylate selected from the group consisting of n-propyl-, n-butyl, n-octyl, 2-ethylhexyl-, and 2-methoxethyl-acrylates. The preferred alkyl acrylates are n-butyl-, 2-ethylhexyl-, and 2-methoxyethyl-acrylates. The softening comonomer can also be an alkyl vinyl ether selected from the group consisting of n-butyl, n-hexyl, 2-ethylhexyl-, and 2-methoxyethyl-vinyl ether. The preferred alkyl vinyl ethers are n-butyl vinyl ether and n-hexyl vinyl ether. The coplymer is about 10 to 70% neutralized with metal ions selected from groups Ia, Ib, Ia, IIIa, IVa, VIb, and VIII of the Periodic Table of Elements such as sodium, potassium zinc, calcium, magnesium, lithium, aluminum, nickel, and chrominum. Preferably the copolymer has from about 35 to about 70% of the carboxylic acid groups ionized by neutralization with metal ions selected from the group consisting of sodium, potassium, zinc, calcium, and magnesium. Component (c) is present in the composition of the present invention in amounts of 10-25 wt. %, preferably 15-20 wt. %.
The copolymer of ethylene and glycidyl acrylate or ethylene and glycidyl methacrylate (component (d)) preferably contains copolymerized units of an alkyl acrylate or an alkyl methacrylate having 1-6 carbon atoms. The ethylene/glycidyl acrylate or ethylenel-glycidyl methacrylate copolymer contains 60-88 weight percent ethylene and 1-12 weight percent glycidyl acrylate or glycidyl methacrylate. Representative alkyl acrylates and alkyl methacrylates that are used in the copolymer include methyl acrylate, ethyl acrylate, propyl acrylate, n-butyl acrylate, isobutyl acrylate, hexyl acrylate, methyl methacrylate, ethyl methacrylate, propyl methacrylate, butyl methacrylate, and hexyl methacrylate. Ethyl acrylate is preferred and n-butyl a

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