WO2002066555A2 - Low tg ethylene-based polymer, cycloolefin polymer blends - Google Patents

Low tg ethylene-based polymer, cycloolefin polymer blends Download PDF

Info

Publication number
WO2002066555A2
WO2002066555A2 PCT/US2002/008149 US0208149W WO02066555A2 WO 2002066555 A2 WO2002066555 A2 WO 2002066555A2 US 0208149 W US0208149 W US 0208149W WO 02066555 A2 WO02066555 A2 WO 02066555A2
Authority
WO
WIPO (PCT)
Prior art keywords
weight
blend
polymer
ethylene
based polymer
Prior art date
Application number
PCT/US2002/008149
Other languages
French (fr)
Other versions
WO2002066555A3 (en
Inventor
Karlheinz Hausmann
Original Assignee
E.I. Dupont De Nemours And Company
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by E.I. Dupont De Nemours And Company filed Critical E.I. Dupont De Nemours And Company
Priority to JP2002566267A priority Critical patent/JP2004522842A/en
Priority to EP02717655A priority patent/EP1401952A2/en
Priority to AU2002248642A priority patent/AU2002248642A1/en
Publication of WO2002066555A2 publication Critical patent/WO2002066555A2/en
Publication of WO2002066555A3 publication Critical patent/WO2002066555A3/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/04Homopolymers or copolymers of ethene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/04Homopolymers or copolymers of ethene
    • C08L23/08Copolymers of ethene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/04Homopolymers or copolymers of ethene
    • C08L23/08Copolymers of ethene
    • C08L23/0807Copolymers of ethene with unsaturated hydrocarbons only containing more than three carbon atoms
    • C08L23/0815Copolymers of ethene with aliphatic 1-olefins
    • C08L23/0823Copolymers of ethene with aliphatic cyclic olefins
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/04Homopolymers or copolymers of ethene
    • C08L23/08Copolymers of ethene
    • C08L23/0846Copolymers of ethene with unsaturated hydrocarbons containing other atoms than carbon or hydrogen atoms
    • C08L23/0869Acids or derivatives thereof
    • C08L23/0876Neutralised polymers, i.e. ionomers

Definitions

  • This invention relates to blends comprising an ethylene based polymer having a specific glass transition temperature and a cycloolefin polymer, and to their applications in molded articles and films.
  • Cycloolefin polymers have long been used in the preparation of molded articles. But these materials are stiff and brittle. As a consequence, improvement of impact strength, or toughness, of cycloolefin polymers has long been of interest. Resistance to shattering or brittle breaking on impact of molded articles is a desirable feature of any molded article.
  • ductile is meant that sharp cracks in the molded polymer are not initiated, or if initiated do not tend to propagate, from the area of impact. Breaks are characterized more by tearing with a large volume of adjacent material yielding at the edge of the crack or tear rather than a sharp, clean break with little molecular displacement.
  • a polymer having good ductility is one that is resistant to crack propagation caused by impact.
  • a first aspect of the invention is a blend comprising at least an ethylene based polymer having a glass transition temperature lower than or equal to 20°C and at least a cycloolefin polymer.
  • Another aspect of the invention is an article, in particular a molded article, comprising the above blend.
  • Another aspect of the invention is a film comprising the above blend.
  • the blend of the invention allows one to obtain improved mechanical properties of molded article.
  • the first essential component of the invention is a cycloolefin polymer.
  • Suitable cycloolefin polymers for the invention have a mean molecular weight Mw (weight average) in the range from 200 to 100,000. They are substantially amorphous, i.e. have a crystallinity of less than 5% by weight. They preferably show a glass transition temperature Tg, which is generally in the range from 0 to 300°C.
  • the polydispersity Mw/Mn of the cycloolefin polymers is preferably from 1 to 5.
  • Cycloolefin polymers are homopolymers built up from only one type of cycloolefins or copolymers built up from cycloolefins and comonomers (COCs), where the comonomer content is at most 20% by weight, based on the weight of the cycloolefin polymer.
  • Cycloolefins are mono or polyunsaturated polycyclic ring systems, such as cycloalkenes, bicycloalkenes, tricycloalkenes or tetracycloalkenes. The ring systems can be monosubstituted or polysubstituted.
  • cycloolefins which are built up from monoalkylated or unsubstituted cycloolefins.
  • Particularly preferred cycloolefin homopolymers are polynorbomene, polydimethyloctahydronaphthalene, polycyclopentene and poly(5-methyl)norbornene.
  • the cycloolefin polymers can also be branched. Products of this type can have comb or star structures. If desired, the above-described cycloolefins can also be copolymerized with comonomers.
  • these cycloolefin copolymers contain up to 20% by weight, preferably about 1-15% by weight, in particular about 1-8% by weight, based on the weight of the COC, of comonomer.
  • Preferred comonomers are olefins having 2 to 6 carbon atoms, in particular ethylene and butylene.
  • Preferred cycloolefin polymers of the invention are ethylene- norbomene copolymers.
  • the cycloolefin polymers can be prepared with the aid of transition-metal catalysts. Preparation processes are described, for example, in DD-A-109 225, EP-A-0 407 870, EP-A-0 485 893 and US 5,869,586, US 6,068,936 and WO98/27126 which are incorporated herein by way of reference.
  • Molecular weight regulation during the preparation can advantageously be effected using hydrogen. Suitable molecular weights can also be established through targeted selection of the catalyst and reaction conditions. Details in this respect are given in the above mentioned specifications.
  • Suitable cycloolefin for the invention are the products sold under the trademark Topas® by Ticona.
  • the cycloolefin polymer is usually present in the blend of the invention in an amount from 50 weight % to about 99.9 %, relative to the weight of the blend.
  • the second essential component of the composition of the invention is an ethylene based polymer having a glass transition temperature or Tg lower than or equal to 20°C, more preferably lower than or equal to 0°C. Tg is measured through thermomechanical analysis according to ASTM D 3418.
  • This ethylene based polymer is preferably a copolymer or a terpolymer.
  • the ethylene based polymer of the invention preferably comprises ethylene and a comonomer selected from the group of carboxylic acids, alkyl acrylates and alpha-olefins.
  • Preferred alpha-olefins are selected from the ones having 3-20 carbon atoms, more preferably from the group of 1-pentene, 1-hexene, 4-methyl-1-pentene, 1-octene, 1-decene, 1-dodecene, 1-butene and 1-octene such as described in US Patent Nos. 5,272,236, 5,278,272 and in WO 94/06817. Most preferably, alpha-olefins have 4-8 carbon atoms. Most preferred alpha-olefins are selected from the group of 1-butene, 1-hexen and 1-octene.
  • the ethylene based polymer is polar, that is to say that it is an ethylene based polymer where part of the hydrogen atoms in the hydrocarbon chain of polyethylene is substituted by at least one atom chosen from oxygen or nitrogen.
  • the ethylene monomer is preferably present in an amount of at least 60 weight %, relative to the weight of the polymer.
  • the ethylene based polymer is of ethylene, ⁇ , ⁇ -ethylenically unsaturated C3-C8 carboxylic acid, and optionally one or more softening comonomers copolymerizable with ethylene.
  • the ⁇ . ⁇ -ethylenically unsaturated C3-C8 carboxylic acid is preferably present in an amount of 5-15 weight %, relative to the weight of the polymer.
  • the softening monomer is preferably present in an amount of less than 25 weight %, relative to the weight of the polymer.
  • Acrylic and methacrylic acids are preferred acid comonomers.
  • the softening comonomer can be an alkyl acrylate selected from the group consisting of methyl acrylate, n-propyl-, iso-butyl-, n-butyl-, n-octyl-,
  • the preferred alkyl acrylates are iso-butyl-, 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 polymer is optionally about 0.01 to 99.5% neutralized with metal ions selected from groups la, lb, lla, Ilia, IVa, Vlb, and VIII of the Periodic Table of Elements such as sodium, potassium, zinc, calcium, magnesium, lithium, aluminum, nickel, and chromium.
  • metal ions selected from groups la, lb, lla, Ilia, IVa, Vlb, and VIII of the Periodic Table of Elements such as sodium, potassium, zinc, calcium, magnesium, lithium, aluminum, nickel, and chromium.
  • Such neutralized ethylene acid copolymers are known in the art as Monomers'. Typically, neutralization will be from 10-70%.
  • 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, lonomers and their methods of manufacture are described in US Patent No. 3,264,272.
  • Suitable polymers for use in the present invention are the ionomers commercially available under the trademark Surlyn® from E. I. du Pont de Nemours and Company and the ethylene acid copolymers available under the trademark Nucrel® from E. I. du Pont de Nemours and Company.
  • the ethylene based polymer is of ethylene, alkyl (meth)acrylate and optionally one vinylalkylsilane termonomer.
  • the alkyl (meth)acrylate monomer is preferably present in an amount of 5-40 weight %, relative to the weight of the polymer.
  • the vinylalkylsilane termonomer is preferably present in an amount of less than 3 weight %, relative to the weight of the polymer.
  • the alkyl group of the alkyl (meth)acrylate monomer is preferably methyl but can be a higher alkyl group up to octyl.
  • the preferred vinylalkylsilane termonomers are vinylmethylsilane and vinylethylsilane.
  • Suitable polymers for use in the present invention are the products commercially available under the trademark Elvaloy® AC from E. I. du Pont de Nemours. These polymers can be prepared by the various methods known in the art such as high pressure free radical polymerization.
  • the ethylene based polymer is usually present in the blend of the invention in an amount from about 0.1 weight % to 50 weight %, relative to the weight of the blend.
  • the blends of the invention may comprise the usual additives including plasticizers, stabilizers, antioxidants, ultraviolet ray-absorbers, hydrolytic stabilizers, anti-static agents, dyes or pigments, fillers, fire- retardants, lubricants, reinforcing agents such as glass fiber and flakes, processing aids, for example release agents, and/or mixtures thereof.
  • the blend of the invention can be prepared by any extrusion process, for instance in the following manner : a blend is prepared by simply mixing the dry components, as a salt and pepper blend ⁇ This blend is then compounded in an extruder. The exiting compound is granulated.
  • the molded article is prepared as follows : the blend obtained from the compounding step in the extruder is fed into a molding machine. Parts in different shapes are injected under high pressure from the molten polymer.
  • the film of the invention can be prepared by extrusion as follows : the granulates obtained as hereinabove are melted in a suitable extruder and converted into a film with at least one individual layer using a converting technique.
  • Suitable converting techniques are for instance blown film extrusion, cast sheet extrusion, extrusion coating.
  • TOPAS® 8007 copolymer of ethylene and norbornene, commercially sold by TICONA
  • TOPAS® 6013 copolymer of ethylene and norbornene, commercially sold by TICONA
  • lonomer 1 copolymer with ethylene, 10% methacrylic acid and 10% i-butylacrylate, MFI (melt flow index) of 1 , 36% neutralized with Na, commercially available from E. I. du Pont de Nemours and Company.
  • lonomer 2 copolymer with ethylene, 10% methacrylic acid and 10% i-butylacrylate, MFI of 1 , 73% neutralized with Zn, commercially available from E. I. du Pont de Nemours and Company.
  • Elvaloy® AC 2116 copolymer of ethylene and 16% ethylacrylate , MFI of 1 , commercially available from E. I. du Pont de Nemours and Company.
  • MFI Melt Flow Index
  • compositions were prepared. All amounts are given in parts by weight relative to the total weight of the composition.
  • compositions are compounded in a 24 mm PRISM twin screw extruder using a high shear screw. All ingredients were prepared as a salt and pepper blend and granulated after exiting the extruder.
  • the compounding temperature conditions were as such:
  • the granulates obtained above are melted in Brabender 24mm single screw extruder where 1mm thick sheets are extruded.
  • the melting temperature of the Brabender single screw extruder was as follows: Feed Zone 1 Zone 2 Zone 3 Die Melt
  • the Gardner Impact corresponds to the quantity of energy which is necessary to break the sheet. In consequence, the greater the value of the Gardner impact, the more resistant to impact the sheet. It is clear from these results that the introduction of 20% of an ethylene based polymer according to the invention to a composition of cycloolefin polymer increases the impact resistance of the sheet made of said composition.
  • the granulates obtained above were melted in a RAY RAM injection molding press for test samples at 240°C/8.5 bars into Izod bars of the dimension 80 mm x 10 mm, which were subsequently mechanically notched in order to produce samples according to ISO 180. These samples were tested at room temperature (about 23°C) on an instrumented impact tester of the type CEAST 6548 with a pendulum J2.

Abstract

Blends comprising an ethylene based polymer having a glass transition temperature lower than or equal to 20°C and cycloolefin polymer are prepared. The ethylene based polymer preferably comprises at least 60 weight % of ethylene, relative to the weight of the polymer and polar monomers selected from the group of carboxylic acids, alkyl acrylates and vinyl acetates. It is preferably 0.01 to about 99.5% neutralized with metal ions selected from sodium, potassium, zinc, calcium, magnesium, lithium, aluminum, nickel, and chromium. The cycloolefin polymer is preferably an ethylene-norbornene copolymer. The invention also relates to the applications of such blends to improved impact resistant molded articles.

Description

TITLE
Low Tg Ethylene-based Polymer, Cycloolefin Polymer Blends
Field of Invention
This invention relates to blends comprising an ethylene based polymer having a specific glass transition temperature and a cycloolefin polymer, and to their applications in molded articles and films.
Background of the Invention
Cycloolefin polymers have long been used in the preparation of molded articles. But these materials are stiff and brittle. As a consequence, improvement of impact strength, or toughness, of cycloolefin polymers has long been of interest. Resistance to shattering or brittle breaking on impact of molded articles is a desirable feature of any molded article.
Tendency to break on impact in a brittle fashion is a significant limitation on the usefulness of such articles. By " ductile" is meant that sharp cracks in the molded polymer are not initiated, or if initiated do not tend to propagate, from the area of impact. Breaks are characterized more by tearing with a large volume of adjacent material yielding at the edge of the crack or tear rather than a sharp, clean break with little molecular displacement. A polymer having good ductility is one that is resistant to crack propagation caused by impact.
It would therefore be useful to provide a cycloolefin polymer based composition flexible enough to be more resistant to impact when under the form of molded articles or under the form of extruded films.
Summary of the invention
Now, it has been surprisingly found that the incorporation of an ethylene based polymer having a specific glass transition temperature into a composition comprising a cycloolefin polymer increases the impact resistance of molded articles made from said composition. A first aspect of the invention is a blend comprising at least an ethylene based polymer having a glass transition temperature lower than or equal to 20°C and at least a cycloolefin polymer.
Another aspect of the invention is an article, in particular a molded article, comprising the above blend.
Another aspect of the invention is a film comprising the above blend.
The blend of the invention allows one to obtain improved mechanical properties of molded article.
Detailed description of the invention
The first essential component of the invention is a cycloolefin polymer. Suitable cycloolefin polymers for the invention have a mean molecular weight Mw (weight average) in the range from 200 to 100,000. They are substantially amorphous, i.e. have a crystallinity of less than 5% by weight. They preferably show a glass transition temperature Tg, which is generally in the range from 0 to 300°C. The polydispersity Mw/Mn of the cycloolefin polymers is preferably from 1 to 5.
Cycloolefin polymers (COPs) are homopolymers built up from only one type of cycloolefins or copolymers built up from cycloolefins and comonomers (COCs), where the comonomer content is at most 20% by weight, based on the weight of the cycloolefin polymer. Cycloolefins are mono or polyunsaturated polycyclic ring systems, such as cycloalkenes, bicycloalkenes, tricycloalkenes or tetracycloalkenes. The ring systems can be monosubstituted or polysubstituted. Preference is given to the cycloolefins which are built up from monoalkylated or unsubstituted cycloolefins. Particularly preferred cycloolefin homopolymers are polynorbomene, polydimethyloctahydronaphthalene, polycyclopentene and poly(5-methyl)norbornene. The cycloolefin polymers can also be branched. Products of this type can have comb or star structures. If desired, the above-described cycloolefins can also be copolymerized with comonomers. In a preferred embodiment of the invention, these cycloolefin copolymers (COCs) contain up to 20% by weight, preferably about 1-15% by weight, in particular about 1-8% by weight, based on the weight of the COC, of comonomer. Preferred comonomers are olefins having 2 to 6 carbon atoms, in particular ethylene and butylene.
Preferred cycloolefin polymers of the invention are ethylene- norbomene copolymers.
The cycloolefin polymers can be prepared with the aid of transition-metal catalysts. Preparation processes are described, for example, in DD-A-109 225, EP-A-0 407 870, EP-A-0 485 893 and US 5,869,586, US 6,068,936 and WO98/27126 which are incorporated herein by way of reference. Molecular weight regulation during the preparation can advantageously be effected using hydrogen. Suitable molecular weights can also be established through targeted selection of the catalyst and reaction conditions. Details in this respect are given in the above mentioned specifications.
Suitable cycloolefin for the invention are the products sold under the trademark Topas® by Ticona.
The cycloolefin polymer is usually present in the blend of the invention in an amount from 50 weight % to about 99.9 %, relative to the weight of the blend.
The second essential component of the composition of the invention is an ethylene based polymer having a glass transition temperature or Tg lower than or equal to 20°C, more preferably lower than or equal to 0°C. Tg is measured through thermomechanical analysis according to ASTM D 3418. This ethylene based polymer is preferably a copolymer or a terpolymer. The ethylene based polymer of the invention preferably comprises ethylene and a comonomer selected from the group of carboxylic acids, alkyl acrylates and alpha-olefins. Preferred alpha-olefins are selected from the ones having 3-20 carbon atoms, more preferably from the group of 1-pentene, 1-hexene, 4-methyl-1-pentene, 1-octene, 1-decene, 1-dodecene, 1-butene and 1-octene such as described in US Patent Nos. 5,272,236, 5,278,272 and in WO 94/06817. Most preferably, alpha-olefins have 4-8 carbon atoms. Most preferred alpha-olefins are selected from the group of 1-butene, 1-hexen and 1-octene.
In a preferred embodiment of the invention, the ethylene based polymer is polar, that is to say that it is an ethylene based polymer where part of the hydrogen atoms in the hydrocarbon chain of polyethylene is substituted by at least one atom chosen from oxygen or nitrogen. The ethylene monomer is preferably present in an amount of at least 60 weight %, relative to the weight of the polymer.
In a preferred embodiment of the invention, the ethylene based polymer is of ethylene, α,β-ethylenically unsaturated C3-C8 carboxylic acid, and optionally one or more softening comonomers copolymerizable with ethylene. The α.β-ethylenically unsaturated C3-C8 carboxylic acid is preferably present in an amount of 5-15 weight %, relative to the weight of the polymer. The softening monomer is preferably present in an amount of less than 25 weight %, relative to the weight of the polymer. Acrylic and methacrylic acids are preferred acid comonomers. The softening comonomer can be an alkyl acrylate selected from the group consisting of methyl acrylate, n-propyl-, iso-butyl-, n-butyl-, n-octyl-,
2-ethylhexyk and 2-methoxyethyl-acrylates. The preferred alkyl acrylates are iso-butyl-, 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 polymer is optionally about 0.01 to 99.5% neutralized with metal ions selected from groups la, lb, lla, Ilia, IVa, Vlb, and VIII of the Periodic Table of Elements such as sodium, potassium, zinc, calcium, magnesium, lithium, aluminum, nickel, and chromium. Such neutralized ethylene acid copolymers are known in the art as Monomers'. Typically, neutralization will be from 10-70%. 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, lonomers and their methods of manufacture are described in US Patent No. 3,264,272.
Suitable polymers for use in the present invention are the ionomers commercially available under the trademark Surlyn® from E. I. du Pont de Nemours and Company and the ethylene acid copolymers available under the trademark Nucrel® from E. I. du Pont de Nemours and Company.
In another preferred embodiment of the invention, the ethylene based polymer is of ethylene, alkyl (meth)acrylate and optionally one vinylalkylsilane termonomer. The alkyl (meth)acrylate monomer is preferably present in an amount of 5-40 weight %, relative to the weight of the polymer. The vinylalkylsilane termonomer is preferably present in an amount of less than 3 weight %, relative to the weight of the polymer. The alkyl group of the alkyl (meth)acrylate monomer is preferably methyl but can be a higher alkyl group up to octyl. The preferred vinylalkylsilane termonomers are vinylmethylsilane and vinylethylsilane. Suitable polymers for use in the present invention are the products commercially available under the trademark Elvaloy® AC from E. I. du Pont de Nemours. These polymers can be prepared by the various methods known in the art such as high pressure free radical polymerization.
The ethylene based polymer is usually present in the blend of the invention in an amount from about 0.1 weight % to 50 weight %, relative to the weight of the blend.
The blends of the invention may comprise the usual additives including plasticizers, stabilizers, antioxidants, ultraviolet ray-absorbers, hydrolytic stabilizers, anti-static agents, dyes or pigments, fillers, fire- retardants, lubricants, reinforcing agents such as glass fiber and flakes, processing aids, for example release agents, and/or mixtures thereof.
The blend of the invention can be prepared by any extrusion process, for instance in the following manner : a blend is prepared by simply mixing the dry components, as a salt and pepper blendτ This blend is then compounded in an extruder. The exiting compound is granulated.
The molded article is prepared as follows : the blend obtained from the compounding step in the extruder is fed into a molding machine. Parts in different shapes are injected under high pressure from the molten polymer.
The film of the invention can be prepared by extrusion as follows : the granulates obtained as hereinabove are melted in a suitable extruder and converted into a film with at least one individual layer using a converting technique. Suitable converting techniques are for instance blown film extrusion, cast sheet extrusion, extrusion coating.
The invention will be further described in the following Examples.
Examples
Description of ingredients:
Materials used in the Examples set forth below are as follows, identified by the respective trademarks and trade designations :
TOPAS® 8007 : copolymer of ethylene and norbornene, commercially sold by TICONA
TOPAS® 6013 : copolymer of ethylene and norbornene, commercially sold by TICONA
lonomer 1 : copolymer with ethylene, 10% methacrylic acid and 10% i-butylacrylate, MFI (melt flow index) of 1 , 36% neutralized with Na, commercially available from E. I. du Pont de Nemours and Company.
lonomer 2 : copolymer with ethylene, 10% methacrylic acid and 10% i-butylacrylate, MFI of 1 , 73% neutralized with Zn, commercially available from E. I. du Pont de Nemours and Company. Elvaloy® AC 2116 : copolymer of ethylene and 16% ethylacrylate , MFI of 1 , commercially available from E. I. du Pont de Nemours and Company.
The Melt Flow Index (MFI) of the above compounds is measured according to ASTM D 1238 @ 190°C/2.16kg
The following compositions were prepared. All amounts are given in parts by weight relative to the total weight of the composition.
Figure imgf000008_0001
The compositions are compounded in a 24 mm PRISM twin screw extruder using a high shear screw. All ingredients were prepared as a salt and pepper blend and granulated after exiting the extruder.
The compounding temperature conditions were as such:
Feed Zone 1 Zone 2 Zone 3 Die Melt
200 225 230 230 230 230
Gardner Impact test
The granulates obtained above are melted in Brabender 24mm single screw extruder where 1mm thick sheets are extruded. The melting temperature of the Brabender single screw extruder was as follows: Feed Zone 1 Zone 2 Zone 3 Die Melt
180 195 225 240 240 240
These sheets were subsequently tested for their impact resistance by a GARDNER falling weight test according to ISO 6603/1 with 250g weight at room temperature.
The results are collected in the following table
Figure imgf000009_0001
The Gardner Impact corresponds to the quantity of energy which is necessary to break the sheet. In consequence, the greater the value of the Gardner impact, the more resistant to impact the sheet. It is clear from these results that the introduction of 20% of an ethylene based polymer according to the invention to a composition of cycloolefin polymer increases the impact resistance of the sheet made of said composition.
Notched Izod test
The granulates obtained above were melted in a RAY RAM injection molding press for test samples at 240°C/8.5 bars into Izod bars of the dimension 80 mm x 10 mm, which were subsequently mechanically notched in order to produce samples according to ISO 180. These samples were tested at room temperature (about 23°C) on an instrumented impact tester of the type CEAST 6548 with a pendulum J2.
The results are collected in the following table :
Figure imgf000009_0002
The greater the Notched Izod value, the more resistant to impact the molded bar.
It is clear from these results that addition of the ethylene based polymer of the invention to cycloolefin polymers significantly increases the impact resistance of molded articles made from cycloolefin polymers based composition.

Claims

CLAIMSWhat is claimed is :
1. A blend comprising at least an ethylene based polymer having a glass transition temperature lower than or equal to 20°C and at least a cycloolefin polymer.
2. The blend of claim 1 , wherein the cycloolefin polymer is built up from cycloolefins and comonomers, where the comonomer content is at most 20% by weight, based on the weight of the cycloolefin polymer.
3. The blend of claim 2, wherein the cycloolefin polymer is an ethylene-norbornene copolymer.
4. The blend of claim 1, wherein the cycloolefin polymer is present in an amount from 50 weight % to about 99.9 weight %, relative to the weight of the blend.
5. The blend of claim 1 , wherein the ethylene based polymer has a glass transition temperature lower than or equal to 0°C.
6. The blend of claim 1 , wherein the ethylene based polymer comprises at least 60 weight % of ethylene, relative to the weight of the polymer and polar monomers selected from the group of carboxylic acids and alkyl acrylates.
7. The blend of claim 1 , wherein the ethylene based polymer is 0.01 to about 99.5% neutralized with metal ions selected from sodium, potassium, zinc, calcium, magnesium, lithium, aluminum, nickel, and chromium.
8. The blend of claim 1 , wherein the ethylene based polymer is present in an amount from about 0.1 weight % to 50%, relative to the weight of the blend.
9. A molded article comprising the blend of claim 8.
10. A film comprising the blend of claim 8.
11. A method for improving the impact resistance of a molded article made of a cycloolefin polymer comprising the step of introducing therein from about 0.1 to 50% by weight, relative of the weight of the article, of an ethylene based polymer having a glass transition temperature lower than or equal to 20°C.
PCT/US2002/008149 2001-02-20 2002-02-20 Low tg ethylene-based polymer, cycloolefin polymer blends WO2002066555A2 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP2002566267A JP2004522842A (en) 2001-02-20 2002-02-20 Blends of low glass transition temperature ethylene-based polymer and COCLOOLEFIN polymer
EP02717655A EP1401952A2 (en) 2001-02-20 2002-02-20 Low glass transition temperature ethylene-based polymer, cycloolefin polymer blends
AU2002248642A AU2002248642A1 (en) 2001-02-20 2002-02-20 Low tg ethylene-based polymer, cycloolefin polymer blends

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US26990201P 2001-02-20 2001-02-20
US60/269,902 2001-02-20

Publications (2)

Publication Number Publication Date
WO2002066555A2 true WO2002066555A2 (en) 2002-08-29
WO2002066555A3 WO2002066555A3 (en) 2003-11-27

Family

ID=23029100

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2002/008149 WO2002066555A2 (en) 2001-02-20 2002-02-20 Low tg ethylene-based polymer, cycloolefin polymer blends

Country Status (5)

Country Link
US (1) US6696524B2 (en)
EP (1) EP1401952A2 (en)
JP (1) JP2004522842A (en)
AU (1) AU2002248642A1 (en)
WO (1) WO2002066555A2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8541077B2 (en) 2005-11-15 2013-09-24 Dow Global Technologies Llc Oriented multi-layer shrink labels

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7265183B2 (en) 2004-11-01 2007-09-04 Ticona Llc High clarity, low friction polyethylene compositions for films
US8344070B2 (en) * 2006-08-04 2013-01-01 Exxonmobil Chemical Patents Inc. Polymer compositions comprising cyclic olefin polymers, polyolefin modifiers, and fillers
US20080033112A1 (en) * 2006-08-04 2008-02-07 Squire Kevin R Polymer compositions comprising cyclic olefin copolymers and polyolefin modifiers
US8148472B1 (en) 2006-08-04 2012-04-03 Exxonmobil Research And Engineering Company Polymer compositions comprising cyclic olefin polymers, polyolefin modifiers and non-functionalized plasticizers
US8519056B2 (en) * 2007-06-01 2013-08-27 Exxonmobil Chemical Patents Inc. Blends of co-precipitated hydrogenated ethylene-dicyclpentadiene and elastomeric polymers to provide impact modified structural polyolefins
JP5134868B2 (en) * 2007-06-15 2013-01-30 アキレス株式会社 Olefin resin film
JP5775400B2 (en) * 2011-09-02 2015-09-09 三井・デュポンポリケミカル株式会社 α-Olefin / Cyclic Olefin Copolymer Composition and Molded Body
JP5844138B2 (en) * 2011-12-22 2016-01-13 三井・デュポンポリケミカル株式会社 Flooring
CN106574071B (en) 2014-08-21 2020-05-29 W·W·严 Microporous sheet products and methods of making and using the same
WO2016073580A1 (en) 2014-11-05 2016-05-12 William Winchin Yen Microporous sheet product and methods for making and using the same
EP3216068A4 (en) 2014-11-05 2018-04-25 Yen, William Winchin Microporous sheet product and methods for making and using the same

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5166250A (en) * 1990-03-26 1992-11-24 Atochem Flame-retardant ethylene polymer compositions and protective sheathing of electrical cables therewith
EP0597119A1 (en) * 1992-05-26 1994-05-18 Mitsui Petrochemical Industries, Ltd. Cycloolefin copolymer composition and production thereof
EP1234854A1 (en) * 2000-04-28 2002-08-28 Mitsui Chemicals, Inc. Molded object of thermoplastic resin and composition
WO2002066495A2 (en) * 2001-02-20 2002-08-29 E.I. Dupont De Nemours And Company Polar ethylene-based polymer, cycloolefin polymer blends

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL128027C (en) 1961-08-31 1900-01-01
DD109225A1 (en) 1973-07-19 1974-10-20
DE68927491T2 (en) * 1988-09-30 1997-03-27 Mitsui Petrochemical Ind Disordered cycloolefin copolymer composition and its reaction product
DE3922546A1 (en) 1989-07-08 1991-01-17 Hoechst Ag METHOD FOR THE PRODUCTION OF CYCLOOLEFINPOLYMERS
US5272236A (en) 1991-10-15 1993-12-21 The Dow Chemical Company Elastic substantially linear olefin polymers
US5371158A (en) 1990-07-05 1994-12-06 Hoechst Aktiengesellschaft Bulk polymerization using specific metallocene catalysts for the preparation of cycloolefin polymers
TW227005B (en) 1990-11-14 1994-07-21 Hoechst Ag
US5278272A (en) 1991-10-15 1994-01-11 The Dow Chemical Company Elastic substantialy linear olefin polymers
US5389515A (en) 1992-09-15 1995-02-14 Boehringer Mannheim Corporation Isolated nucleotide sequences for identifying Neisseria gonorrhoeae
DE19536043A1 (en) 1995-09-28 1997-04-10 Hoechst Ag Polyolefin film with cycloolefin polymer, process for its production and its use
DE19546500A1 (en) 1995-12-13 1997-06-19 Hoechst Ag Production of cyclo-olefin copolymers e.g. for pipes
DE19652340A1 (en) 1996-12-17 1998-06-18 Hoechst Ag Process for the preparation of cycloolefin copolymers

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5166250A (en) * 1990-03-26 1992-11-24 Atochem Flame-retardant ethylene polymer compositions and protective sheathing of electrical cables therewith
EP0597119A1 (en) * 1992-05-26 1994-05-18 Mitsui Petrochemical Industries, Ltd. Cycloolefin copolymer composition and production thereof
EP1234854A1 (en) * 2000-04-28 2002-08-28 Mitsui Chemicals, Inc. Molded object of thermoplastic resin and composition
WO2002066495A2 (en) * 2001-02-20 2002-08-29 E.I. Dupont De Nemours And Company Polar ethylene-based polymer, cycloolefin polymer blends

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8541077B2 (en) 2005-11-15 2013-09-24 Dow Global Technologies Llc Oriented multi-layer shrink labels

Also Published As

Publication number Publication date
US6696524B2 (en) 2004-02-24
US20020161128A1 (en) 2002-10-31
JP2004522842A (en) 2004-07-29
EP1401952A2 (en) 2004-03-31
AU2002248642A1 (en) 2002-09-04
WO2002066555A3 (en) 2003-11-27

Similar Documents

Publication Publication Date Title
CA1193376A (en) Production of polyolefin copolymer
KR100221752B1 (en) Thermoplastic polymer alloy composition
KR100330606B1 (en) Blends of graft-modified substantially linear ethylene polymers and other thermoplastic polymers
JP4462641B2 (en) Novel ionomers based on copolymers of ethylene containing both monocarboxylic and dicarboxylic acids and polyamide blends containing such ionomers
US6696524B2 (en) Low Tg ethylene-based polymer, cycloolefin polymer blends
US7935765B2 (en) Miscible blends of ethylene copolymers with improved temperature resistance
KR920001234B1 (en) Ethylene polymer composition for producing film
EP1423408B1 (en) Polar ethylene-based polymer, cycloolefin polymer blends
KR100526371B1 (en) Elastomer Compositions Having Improved Abrasion Resistance, Coefficient of Friction and Hot Green Strength
FI115530B (en) Copolymers of ethylene and alkyl acrylate and processes for their preparation
EP0748354A1 (en) Flexible polar thermoplastic polyolefin compositions
CN101932657B (en) Method for producing resin composition and molded article
CN101663353A (en) blends of polyolefins, polar ethylene copolymers and functionalized ethylene copolymers
US6077906A (en) Nylon modifiers hauling enhanced flow properties
JPS6351451B2 (en)
JPH02127468A (en) Reinforced nylon scarcely causing mold deposite
CA1252239A (en) Thermoplastic resin composition
EP1148095A1 (en) Thermoplastic resin composition comprising rubber-reinforced styrenic resin and its extrusion moldings
JP3764126B2 (en) Ionomer composition
JPH06299040A (en) Thermoplastic resin composition
MXPA99008180A (en) Elastomer compositions having improved abrasion resistance, coefficient of friction and hot green strength
JPH0797498A (en) Resin composition

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A2

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NO NZ OM PH PL PT RO RU SD SE SG SI SK SL TJ TM TN TR TT TZ UA UG UZ VN YU ZA ZM ZW

AL Designated countries for regional patents

Kind code of ref document: A2

Designated state(s): GH GM KE LS MW MZ SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
WWE Wipo information: entry into national phase

Ref document number: 2002717655

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 02805248X

Country of ref document: CN

Ref document number: 2002566267

Country of ref document: JP

REG Reference to national code

Ref country code: DE

Ref legal event code: 8642

WWP Wipo information: published in national office

Ref document number: 2002717655

Country of ref document: EP

WWW Wipo information: withdrawn in national office

Ref document number: 2002717655

Country of ref document: EP