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EP0548213A1 - Compositions polymeres olefiniques antistatiques contenant des copolymeres d'oxyde d'ethylene et procede associe - Google Patents

Compositions polymeres olefiniques antistatiques contenant des copolymeres d'oxyde d'ethylene et procede associe

Info

Publication number
EP0548213A1
EP0548213A1 EP19910916744 EP91916744A EP0548213A1 EP 0548213 A1 EP0548213 A1 EP 0548213A1 EP 19910916744 EP19910916744 EP 19910916744 EP 91916744 A EP91916744 A EP 91916744A EP 0548213 A1 EP0548213 A1 EP 0548213A1
Authority
EP
European Patent Office
Prior art keywords
ethylene oxide
composition
olefinic
component
oxide copolymer
Prior art date
Legal status (The legal status 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 status listed.)
Withdrawn
Application number
EP19910916744
Other languages
German (de)
English (en)
Inventor
Simon Hsiao-Pao Yu
Thomas Ray Mass
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Goodrich Corp
Original Assignee
BF Goodrich Corp
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 BF Goodrich Corp filed Critical BF Goodrich Corp
Publication of EP0548213A1 publication Critical patent/EP0548213A1/fr
Withdrawn legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02—Compositions 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

Definitions

  • the present invention relates to olefin polymer compositions having improved antistatic properties. More particularly, the olefinic compositions of the present invention comprise an antistatic agent which is preferably a randomly polymerized ethylene oxide copolymer wherein the weight percent of ethylene oxide in the copolymer is about 40 to about 90 weight percent.
  • an antistatic agent which is preferably a randomly polymerized ethylene oxide copolymer wherein the weight percent of ethylene oxide in the copolymer is about 40 to about 90 weight percent.
  • U.S. 3,425,981 to PULETTI et al. is directed to olefin polymer compositions containing ethylene oxide polymers. Although the olefin compositions of PULETTl are taught to exhibit enhanced anti-static properties, the present invention is distinguishable over PULETTl for a number of reasons.
  • homopolymers in olefins do provide some antistatic properties, such olefin compositions are not sufficiently antistatic to meet many of the needs in the marketplace.
  • PULETTl did not appreciate and does not teach or suggest that superior antistatic properties can be obtained by substituting the ethylene oxide homopolymer with a randomly polymerized ethylene oxide copolymer, wherein the comonomers are oxiranes and wherein the amount of ethylene oxide in the copolymer is about 40 to 90 weight percent.
  • PULETTl teaches that the ethylene oxide homopolymer can be substituted with a copolymer, and PULETTI mentions a number of possible comonomers, but the critical copolymer range is not taught or suggested by PULETTI, and PULETTI implies that a copolymer would be a mere alternative to the homopolymer, not a dramatically more effective antistatic additive for olefins.
  • PULETTI teaches that the ethylene oxide polymer component has "an average molecular weight of from 100,000 to ten million and preferably in the range of from about 200,000 to about 1,000,000" (col..2, lines 52-53). Such a molecular weight limitation is not necessary for the present invention, and therefore, Applicant has eliminated an important element of the PULETTI invention, while nevertheless improving antistatic properties of the resulting composition.
  • the present invention is directed to an olefinic composition having antistatic properties and comprising an olefinic component and a random ethylene oxide copolymer component.
  • the ethylene oxide copolymer component preferably comprises about 40 to 90 weight percent of the following polymer unit: (-CH 2 -CH 2 O-).
  • the resulting composition preferably has a surface resistivity in the range of about (10) 10 to about (10) 14 ohm/sq as determined by ASTM D257, and preferably requires less than about 0.5 seconds to dissipate 90% of a 5 kilovolt charge at 50% relative humidity according to National Fire Protection Association Standard (NFPA Code 56A) or requires less than about 2.0 seconds to dissipate 99% of a 5 kilovolt charge at 15% relative humidity according to U.S. Military Specification (MIL-B-81705C) as determined by Federal Test Method Standard 101 B, Method 4046.1.
  • NFPA Code 56A National Fire Protection Association Standard
  • MIL-B-81705C Federal Test Method Standard 101 B, Method 4046.1.
  • the ethylene oxide copolymer preferably comprises about 10 to about 60 weight percent polymer units which are the polymerization product of at least one oxirane comonomer other than ethylene oxide.
  • the oxirane comonomer is most preferably epichlorohydrin or propylene oxide.
  • the olefinic component is a homopolymer or the copolymerization product of an olefin monomer and one or more copolymerizable monomers.
  • the preferred copolymerizable monomers have vinyl functionality.
  • the olefinic component is a derivative of a homopolymer or a copolymer.
  • the olefinic component comprises a blend of an olefin polymer with a second polymer.
  • the olefinic component further comprises a metallic salt functionality.
  • composition of the present invention is a composition of the present invention.
  • the present invention is also directed to a method of manufacturing an antistatic olefinic composition by means of melt mixing or blending the ethylene oxide copolymer of the present invention with an olefinic component.
  • the preferred embodiment of the present invention comprises an olefin component, an ethylene oxide copolymer component, and optionally, any one of a number of conventional additives for olefin type materials.
  • the olefin component is preferably the polymerization product of one or more lower olefin monomers such as those containing from 2 to 8 carbon atoms, most preferably from 2 to 3 carbon atoms.
  • lower olefin monomers such as those containing from 2 to 8 carbon atoms, most preferably from 2 to 3 carbon atoms.
  • Illustrative of such polymers are high density or linear polyethylene, low density or branched polyethylene, polypropylene, polybutene,
  • polycycloolefins polycycloolefins, copolymers of ethylene/pr opylene, copolymers of propylene/butylene, and the like.
  • the olefin component can be the copolymerization product of an olefin monomer and one or more copolymerizable monomers.
  • Preferred comonomers include those having vinyl functionality, such as:
  • vinyl aryls i.e., styrene, o-methoxystyrene, p- methoxystyrene, m-methoxystyrene, o-nitrostyrene, m-nitrostyrene, o-methylstyrene, p-methylstryene, m-methylstyrene, p-phenylstyrene, o-phenylstyrene, m-phenylstyrene, vinylnaphthalene and the like;
  • vinyl and vinylidene halides i.e., vinyl chloride, vinylidene chloride, vinylidene bromide and the like; vinyl esters such as vinyl acetate, vinyl propionate, vinyl butyrate, vinyl chloroacetate, vinyl chloropropionate, vinyl benzoate, vinyl chlorobenzoate and the like; 3.
  • acrylic and alpha-alkyl acrylic acids, their alkyl esters, and their amides i.e., acrylic acid, chloroacrylic acid, methacrylic acid, ethacrylic acid, methyl acrylate, ethyl acrylate, butyl acrylate, n- octyl acrylate, 2-ethylhexyl acrylate, n-decyl acrylate, methyl methacrylate, butyl methacrylate, methyl ethacrylate, ethyl ethacrylate, acrylamide, N- methyl acrylamide, N,N-dimethyl acrylamide, methacrylamide, N-methyl methacrylamide, N,N- dimethyl methacrylamide, and the like;
  • vinyl alkyl esters and ketones i.e., vinyl methyl ether, vinyl ethyl ether, vinyl isobutyl ether, 2- chloroethyl vinyl ether, methyl vinyl ketone, ethyl vinyl ketone, isobutyl vinyl ketone and the like; and
  • olefin copolymer compositions include the polymerization product of the following:
  • styrene/ethylene ethylene/ethyl acrylate; ethylene/vinyl acetate; ethylene/vinyl chloride; ethylene/acrylic acid; and the like.
  • the most preferred olefinic polymers and copolymers are those which exhibit thermoplastic properties, although thermosets are also intended to be included within the scope of this invention.
  • the olefin component can be the product of grafted variations or chemical derivatives of
  • variations or derivatives are chlorinated polyethylene, copolymer of ethylene/vinyl alcohol, and the like.
  • the olefin polymer component can be of the film forming type.
  • Such resins generally exhibit melt indices of from .1 to 20 decigrams per minute inclusive.
  • olefin polymers are the blends of olefin polymers with other polymers.
  • olefin polymers include polyethylene with polypropylene, low density polyethylene with high density polyethylene, polyethylene with olefin copolymers such as these indicated above, for example, ethylene/acrylic acid copolymer, ethylene/methyl acrylate copolymer, ethylene/ethylacrylate copolymer, ethylene/vinyl acetate copolymer, ethylene/acrylic acid/ethyl acrylate
  • olefinic blends within the scope of the present invention include the blends of olefin polymers with one or more elastomers, crosslinked or non-crosslinked.
  • olefin polymers with one or more elastomers are polypropylene/EPDM; polypropylene/NBR;
  • olefin polymers are also included within the blend of olefin polymers.
  • metallic salts of those olefin copolymers or blends which contain free carboxylic acid or sulfonic acid groups are also included within the blend of olefin polymers.
  • ethylene/acrylic acid copolymer is also included within the blend of olefin polymers.
  • polyolefins propylene/acrylic acid copolymer, butene/acrylic acid copolymer and the like.
  • metals which can be used to provide the salts of said carboxylic acid polymers are the one, two, and three valence metals, such as ammonium, sodium, lithium, potassium, calcium, magnesium, aluminum, barium, zinc, zirconium, beryllium, iron, nickel, cobalt, and the like.
  • Preferred blends include polypropylene or polyethylene with copolymer of ethylene/vinyl acetate or chlorinated polyethylene, and the like.
  • the preferred ethylene oxide copolymer component of the compositions of the present invention is selected from ethylene oxide polymeric materials having an average molecular weight of from about 1000 to ten million and more preferably in the range of from about 10,000 to about 500,000, (GPC
  • ethylene oxide copolymers refers to randomly polymerized copolymers wherein the polymerization product comprises about 40 to 90 weight percent of the following polymer unit:
  • the balance of the ethylene oxide copolymer component is preferably one or more oxirane comonomers other than ethylene oxide.
  • oxirane comonomers can be used, but the preferred comonomers are 1,2-epoxides, the most preferred of which are propylene oxide and/or epichlorohydrin.
  • Catalyst residues or the like or other comonomers can intentionally or unintentionally become incorporated into the ethylene oxide copolymer and this generally is acceptable, provided the polymerization product is about 40 to 90 weight percent ethylene oxide. Ordinary skill and experimentation may be necessary to determine the optimal comonomer composition, depending upon the desired properties of the final material.
  • the Antistatic Olefin Composition
  • the ethylene oxide polymer is generally used in an amount sufficient to impart the desired antistatic or electrostatic dissipative properties. These amounts are generally about 2 to 50 weight parts ethylene oxide copolymer per hundred weight parts olefin polymer resin. Amounts of from about 10 to about 40 weight parts by weight are most preferred.
  • the ethylene oxide polymer can generally be blended with the olefin polymer by general melt blending techniques utilizing conventional equipment. It facilitates blending however if the resinous components are premixed as dry powders before blending in the melt. If desired, solution admixture can be used.
  • filled polymer compositions of this invention containing from about 5 to about 50 parts by weight finely divided filler per hundred parts olefin polymer provides excellent antistatic properties. For these reasons and the apparent economic advantages, these filled compositions are preferred for these applications where transparency of the polymer is not required.
  • filler particle size of from 0.01 ⁇ to 15 ⁇ can be used.
  • Film forming compositions containing a filler having a particle size of from 0.2 to 6 ⁇ are preferred. In applications other than film, filler size is not critical.
  • fillers such as, barium sulfate, calcium sulfate, silica, fibrous asbestos, talc, calcium silicate, magnesium silicate, mica, soapstone, slate flour, pumice, wood flour, soybean flour, tobacco flour, walnut shell flour, sulfur, tripolite, calcium oxide, magnesium oxide, calcite, diatomaceous earth
  • conductive fillers such as, carbon black, metallic powders and the like.
  • additives as are normally present in the resinous components or normally used in such compositions can be present in the polymer compositions of this invention.
  • additives include resin stabilizers to protect the resinous components from degradation caused by shear, heat, light oxidation and the like and which are usually provided in
  • the antistatic properties of polymer blend composition are determined under controlled conditions at 25°C by surface and volume resistivity at 50% R.H. (relative humidity) and static decay time at 15% R.H.
  • the samples were also conditioned at least 48 hours prior to measurement.
  • electrostatic behavior has been characterized by the Department of Defense in publication DOD-HDBK-263 in terms of surface resistivity. Materials with a surface resistivity in the range of 10 9 -10 14 ohms per square at 50% R.H. are antistatic. Materials with a surface resistivity greater than 10 14 are generally insulators. In another example, electrostatic behavior has also been characterized by EIA
  • Sensitive Items 1988, in terms of surface resistivity. Materials with a surface resistivity in the range of 10 5 - 10 12 ohms per square at 50% R.H. are generally "dissipative". Materials with a surface resistivity equal to or greater than about 10 12 are generally insulative.
  • Static decay is a measure of the ability of a material, when grounded, to dissipate a known charge that has been induced on the surface of the material.
  • a sheet sample (3" x 6") with 1/8- 1/16 inch thickness is placed between clamp electrodes contained in a Faraday cage.
  • the material shall be considered acceptable if the decay rate is less than two seconds from 5000 to 50 volts at 15% R.H.
  • Profax 6323 general purpose injection-mold polypropylene from Himont USA Inc., was mixed with a copolymer of ethylene oxide and epichlorohydrin (EO/ECH) with 80 wt % of EO in a Banbury mixer heated at 195°C with hot oil. After mixing (about 5 min.), a 6" x 6" x 1/8" sheet sample was press-molded at 195°C and 30,000 psi. The results are shown in Table I.
  • Profax SB 222 propylene copolymer from Himont USA Inc., was mixed with a copolymer of EO/ECH with 80 wt% of EO in a Banbury mixer heated at 190°C with hot oil. After mixing (about 5 min.), a 6" x 6" x 1/8 sheet sample was press- molded at 190°C and 30,000 psi. The results are shown in Table II.
  • Profax 6323 general purpose injection-mold polypropylene from Himont USA, Inc. and Tyrin 3611, chlorinated polyethylene from Dow Chemical, were mixed with a copolymer of EO/ECH with 80 wt% of EO in a Banbury mixer heated at 195°C with hot oil. After mixing (about 5 min.), a 6" x 6" x 1/8" sheet sample was press-molded at 195°C and 30,000 psi. The presence of chlorinated polyethylene significantly improves antistatic properties. The results are shown in Table III.
  • LDPE resin resin of ethylene/vinyl acetate copolymer, and a copolymer of EO/ECH or EO/PO with 80 wt% of EO were mixed via standard laboratory banbury/mill mixing techniques.
  • the mixed alloys were stripped off a standard 2 roll mill, were injection molded on a 75 ton Arburg injection molding machine. Molding conditions used were those
  • the alloys were prepared using a 300 mm corotating and in termeshing twin screw compounding extruder. A fairly intensive mixing screw configuration was used to minimize dispersion stock temperatures reached 340 to 350°F (121 to 177°C) during the melt blending operation.
  • Injection molded test specimens were prepared on a 75 ton Arburg injection molding machine. Melt temperatures for molding were in the 330 to 350°F (166 to 177°C range with the mold temperature set at 110°F (43°C).

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

Compositions polymères oléfiniques présentant des propriétés antistatiques améliorées. Plus particulièrement, les compositions oléfiniques de l'invention comprennent un agent antistatique, lequel est de préférence un copolymère d'oxyde d'éthylène polymérisé de manière aléatoire, le pourcentage pondéral d'oxyde d'éthylène dans ledit copolymère étant compris entre environ 40 et environ 90 pourcent en poids.
EP19910916744 1990-09-13 1991-09-10 Compositions polymeres olefiniques antistatiques contenant des copolymeres d'oxyde d'ethylene et procede associe Withdrawn EP0548213A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US58185290A 1990-09-13 1990-09-13
US581852 1990-09-13

Publications (1)

Publication Number Publication Date
EP0548213A1 true EP0548213A1 (fr) 1993-06-30

Family

ID=24326833

Family Applications (1)

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EP19910916744 Withdrawn EP0548213A1 (fr) 1990-09-13 1991-09-10 Compositions polymeres olefiniques antistatiques contenant des copolymeres d'oxyde d'ethylene et procede associe

Country Status (5)

Country Link
EP (1) EP0548213A1 (fr)
JP (1) JPH06500817A (fr)
AU (1) AU8538091A (fr)
CA (1) CA2091461A1 (fr)
WO (1) WO1992005220A1 (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5614589A (en) * 1993-11-15 1997-03-25 Kawasaki Chemical Holding Co., Inc. Transparent, antistatic thermoplastic composition and methods of making the same
EP3274376B1 (fr) 2015-03-26 2018-06-20 Basell Polyolefine GmbH Procédé de polymérisation en présence d'un agent antistatique

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1297341B (de) * 1961-10-31 1969-06-12 Huels Chemische Werke Ag Antielektrostatischmachen von Polymeren
JPS6020964A (ja) * 1983-07-15 1985-02-02 Toyobo Co Ltd 帯電防止性重合体組成物
JPS6197421A (ja) * 1984-10-11 1986-05-15 Toyobo Co Ltd 制電性複合繊維の製造方法
US4719263A (en) * 1985-05-10 1988-01-12 The B. F. Goodrich Company Antistatic plastic materials containing epihalohydrin polymers
EP0282985A3 (fr) * 1987-03-20 1990-09-19 The B.F. Goodrich Company Polymère d'oxyde d'éthylène et d'épihalohydrine comme additif antistatique
CA1318740C (fr) * 1987-04-17 1993-06-01 Simon Hsiao-Pao Yu Copolymeres d'oxyde d'ethylene comme additifs antistatiques

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO9205220A1 *

Also Published As

Publication number Publication date
AU8538091A (en) 1992-04-15
WO1992005220A1 (fr) 1992-04-02
CA2091461A1 (fr) 1992-03-14
JPH06500817A (ja) 1994-01-27

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