WO1999060055A1 - Method for reducing extractable heavy metals (lead) from halogenated polymer compositions - Google Patents

Method for reducing extractable heavy metals (lead) from halogenated polymer compositions Download PDF

Info

Publication number
WO1999060055A1
WO1999060055A1 PCT/US1999/010660 US9910660W WO9960055A1 WO 1999060055 A1 WO1999060055 A1 WO 1999060055A1 US 9910660 W US9910660 W US 9910660W WO 9960055 A1 WO9960055 A1 WO 9960055A1
Authority
WO
WIPO (PCT)
Prior art keywords
lead
composition
polymer
parts
metal phosphate
Prior art date
Application number
PCT/US1999/010660
Other languages
French (fr)
Inventor
Richard F. Grossman
Original Assignee
Hammond Group, Inc.
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 Hammond Group, Inc. filed Critical Hammond Group, Inc.
Priority to AU39909/99A priority Critical patent/AU3990999A/en
Publication of WO1999060055A1 publication Critical patent/WO1999060055A1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/32Phosphorus-containing compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/10Metal compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/09Carboxylic acids; Metal salts thereof; Anhydrides thereof
    • C08K5/098Metal salts of carboxylic acids

Definitions

  • Haiogenated polymers such as chlorinated polyethylene
  • CPE polychloroprene
  • PVC polyvinyl chloride
  • CSPE chlorosulfonated polyethylene
  • Insulated products include residential
  • compositions based on haiogenated polymers typically provide required
  • nonhalogenated polymers e.g., olefin polymers and copolymers
  • compositions based on haiogenated polymers in
  • dibasic lead phthalate dibasic lead phosphite
  • red lead oxide are also used.
  • Toxicity Characteristic Leaching Procedure (TCLP)
  • haiogenated polymers by the TCLP has been an objective in the above
  • the present invention is directed to haiogenated polymer
  • compositions containing heavy metal stabilizers such as lead compounds
  • having a lead stabilizer can be reduced by adding a metal phosphate in an
  • phosphates can be used.
  • the invention provides for greatly reduced extractable lead
  • metal phosphate such as calcium phosphate
  • blends also appear to be less soluble in digestive fluids.
  • the invention is particularly applicable to haiogenated
  • heavy metals such as barium and cadmium, in stabilized haiogenated
  • polyethylene chlorosulfonated polyethylene, polychloroprene, polyvinyl
  • halogen is bonded to the carbon atoms of the carbon chain of the
  • vinylidene chloride polymers vinyl chloride-vinyl ester copolymers, vinyl
  • chloride commonly used in the industry is the chloride, although others such as bromide and fluoride may be used. Examples of the latter polymers
  • the heavy metal can be lead, cadmium or barium, for example.
  • the lead stabilizers comprise litharge, red lead, dibasic lead phthalate,
  • dibasic lead phosphite dibasic lead phosphite, tribasic lead sulfate, tetrabasic lead sulfate,
  • the stabilizers may include heavy metal salts of a
  • carboxylic acid advantageously a C 8 -C 24 carbon link monocarboxylic acid
  • metal phosphate is used hereinafter to
  • the metal salts are alkali or alkaline earth
  • the metal cation is
  • calcium and especially preferred calcium phosphates include CaHP0 4 , mixtures of CaHP0 4 , and Ca 3 (P0 4 ) 2 which are essentially ground
  • Alkali metal phosphates such as Na 2 HP0 4 , can be used.
  • alkali and alkaline metal earth metal phosphates may be included.
  • compositions may be employed in the invention.
  • the metal in general, the metal
  • composition to reduce extractable lead composition to reduce extractable lead.
  • Particularly useful compositions are selected from:
  • compositions of the present invention can also include various additional ingredients
  • hydrocarbon resins or chlorinated olefins or paraffins.
  • Other additives may be used.
  • auxiliary stabilizers include auxiliary stabilizers, antioxidants, light stabilizers, pigments, dyes
  • compositions may optionally contain an inorganic acid
  • hydrotalcites such as various hydrotalcites and Type A hydrous zeolites, or
  • coordinating multidentate metal blend ligands such as 1 ,3-diketone, or
  • antioxidant such as bisphenol A
  • phosphite costabilizer such as
  • diphenyl decyl phosphite diphenyl decyl phosphite. Fillers may be added including coarse ground
  • the cable jacket of Example 1 was made employing the
  • Example 1 The cable jacket of Example 1 was made and the identical
  • Chloropolyethylene wire insulation product consisting of
  • cross linking agents was made. After extrusion and vulcanization, the
  • litharge was replaced with a preblended stabilizer containing 60% by
  • this invention enables the reduction of hazardous waste materials and greatly reduces the cost of
  • Dibasic lead phthalate was found to have an oral LD50 value
  • this invention offers the advantage of
  • compositions containing lead reduce the toxicity in animals where compositions containing lead
  • composition comprising polyvinyl chloride
  • This composition was mixed to a
  • composition of EXAMPLE 8 was mixed using a blend of

Abstract

A metal phosphate is used in halogenated polymer compositions containing heavy metal stabilizers, such as lead, to reduce extractable heavy metals from molded polymer products when tested by the toxicity characteristic leaching procedure (TCLP) of 40 CFR 261.

Description

METHOD FOR REDUCING EXTRACTABLE HEAVY METALS (LEAD) FROM HALOGENATED POLYMER COMPOSITIONS
BACKGROUND OF THE INVENTION
Haiogenated polymers, such as chlorinated polyethylene
(CPE), polychloroprene (CR), polyvinyl chloride (PVC) and
chlorosulfonated polyethylene (CSPE), are commonly used for many
5 useful articles such as wire of cable insulation, electrical component
housings and electrical conductors. Insulated products include residential
and commercial building wire; portable power cord and fixture wires;
automotive primary (harness) wire; telephone and other communications
wires; instrument and appliance wires; motor lead wires, etc.
1 0 Compositions based on haiogenated polymers typically provide required
flame resistance, oil resistance, and resistance to environmental factors
such as ozone and ultraviolet light to a greater extent than would similar
nonhalogenated polymers (e.g., olefin polymers and copolymers) .
Therefore, the use of compositions based on haiogenated polymers in
1 5 useful products is widespread. The wire and cable industry has relied on insulating
haiogenated polymers containing heat stabilizers based on lead
compounds. Thus, electrically insulating CPE and CSPE compositions
usually include dibasic lead phthalate, dibasic lead phosphite, tribasic lead
sulfate, or lead stearate, among others, as heat stabilizers. With
chlorinated polyethylene or chlorosulfonated polyethylene, litharge and
red lead oxide are also used.
On June, 22, 1 990, Part 261 of CFR 40, Protection of
Environment, was amended to include (as Appendix II) Method 1 31 1 ,
Toxicity Characteristic Leaching Procedure (TCLP), as a prerequisite for
any solid waste to be landfilled as nonhazardous waste. When tested per
Method 1 31 1 , the solid waste must yield an extract containing less than
5.0 mg/l of lead. Thus, reduction in the level of lead extractables from
haiogenated polymers by the TCLP has been an objective in the above
mentioned industries.
SUMMARY OF THE INVENTION
The present invention is directed to haiogenated polymer
compositions containing heavy metal stabilizers, such as lead compounds,
having reduced extractable heavy metal. It has been found that the
extractable lead levels of a molded haiogenated polymer composition
having a lead stabilizer can be reduced by adding a metal phosphate in an
effective amount to the polymer composition. In a preferred embodiment the extractable lead of lead-
stabilized CPE, CR, PVC or CSPE polymer is substantially improved by
including a minor amount of about 0.2 to 5 parts, or up to about
20 parts, of a metal phosphate per 1 00 parts of polymer. In particular,
calcium phosphate is preferred. However, other alkali or Group II metal
phosphates can be used.
The invention provides for greatly reduced extractable lead
on exposure of molded compositions to environmental landfill conditions.
In particular, it has been found that a significant reduction of extractable
lead from haiogenated polymer compositions can be achieved by adding
a metal phosphate to the polymer in an effective amount to reduce
extraction of the heavy metals when exposed to the toxicity
characteristic leaching procedure of 40 CFR 261 . The function of the
metal phosphate, such as calcium phosphate, as an additive to reduce
extractable lead from haiogenated polymer compositions is considered
unexpected and surprising. Furthermore, it has been found that the metal
phosphates reduce the toxicity of lead when blended therewith. These
blends also appear to be less soluble in digestive fluids.
The invention is particularly applicable to haiogenated
polymer compositions having lead stabilizers in electric wire or cable
applications. In a broader aspect, the invention is applicable to other
heavy metals, such as barium and cadmium, in stabilized haiogenated
polymer products. The invention in these broader aspects, as well as specific embodiments and other parameters, may be further understood
with reference to the following detailed description.
DETAILED DESCRIPTION OF THE INVENTION
A. Haiogenated Polymer
Halogen-containing polymers or resins which are employed
and which illustrate the principles of this invention include chlorinated
polyethylene, chlorosulfonated polyethylene, polychloroprene, polyvinyl
chloride, and other vinyl halide resin types. Haiogenated polymer or vinyl
halide resin, as understood herein, and as appreciated in the art, are
common terms and are adopted to define those resins or polymers usually
derived by polymerization or copolymerization of vinyl monomers
including vinyl chloride with or without other comonomers such as
ethylene, propylene, vinyl acetate, vinyl ethers, vinylidene chloride,
methacrylate, acrylates, styrene, etc. A simple case is the conversion of
vinyl chloride H2C=CHCI to polyvinyl chloride (CH2C=CHCI)n wherein the
halogen is bonded to the carbon atoms of the carbon chain of the
polymer. Other examples of such vinyl halide resins would include
vinylidene chloride polymers, vinyl chloride-vinyl ester copolymers, vinyl
chloride-vinyl ester copolymers, vinyl chloride-vinyl ether copolymers,
vinyl chloride-vinylidene copolymers, vinyl chloride-propylene copolymers,
chlorinated polyethylene, and the like. Of course, the vinyl halide
commonly used in the industry is the chloride, although others such as bromide and fluoride may be used. Examples of the latter polymers
include polyvinyl bromide, polyvinyl fluoride, and copolymers thereof.
B. Heavy Metal Stabilizers
Heavy metal stabilizers in haiogenated polymer compositions
are well known. These metal compounds serve to capture HCI liberated
during heat processing of the vinyl halide resin composition into its final
shape. The heavy metal can be lead, cadmium or barium, for example.
The lead stabilizers comprise litharge, red lead, dibasic lead phthalate,
dibasic lead phosphite, tribasic lead sulfate, tetrabasic lead sulfate,
tribasic lead maleate, tetrabasic lead fumarate, basic lead carbonate and
dibasic lead stearate. The stabilizers may include heavy metal salts of a
carboxylic acid, advantageously a C8-C24 carbon link monocarboxylic acid
such lauric, oleic, stearic, octoic, or similar fatty acid salts. Mixed metal
salts of such acids, and their preparation, are familiar to those skilled in
the art to which this present invention pertains.
C. Metal Phosphates
The metal phosphates suitable for use in accordance with
the principles of this invention may be derived from a broad ciass of
compounds. In short, the term "metal phosphate" is used hereinafter to
define a member of this class. The metal salts are alkali or alkaline earth
metal, and Group II or lla cations, which are exemplified by calcium,
magnesium, zinc, strontium and barium. Preferably, the metal cation is
calcium and especially preferred calcium phosphates include CaHP04, mixtures of CaHP04, and Ca3(P04)2 which are essentially ground
phosphate rock. Alkali metal phosphates, such as Na2HP04, can be used.
Other alkali and alkaline metal earth metal phosphates may be included.
D. Amounts of Components
Broad ranges of components of the haiogenated polymer
compositions may be employed in the invention. In general, the metal
phosphate is used in an effective amount in the haiogenated polymer
composition to reduce extractable lead. Particularly useful compositions
of the invention are achieved containing about 0.5 to about 5 parts, up
to about 40 parts, of the heavy metal compound heat stabilizer, about
0.2 to about 5 parts, up to about 20 parts, of the metal phosphate, said
parts on the basis of 1 00 parts of the haiogenated polymer. The
compositions of the present invention can also include various additional
compounds including lubricants for providing the polymer or resin with
lubricity and plasticizers of the phthaiic ester or fatty acid ester type,
hydrocarbon resins or chlorinated olefins or paraffins. Other additives may
include auxiliary stabilizers, antioxidants, light stabilizers, pigments, dyes
or extenders. The compositions may optionally contain an inorganic acid
acceptor, such as various hydrotalcites and Type A hydrous zeolites, or
coordinating multidentate metal blend ligands, such as 1 ,3-diketone, or
an antioxidant such as bisphenol A, or a phosphite costabilizer such as
diphenyl decyl phosphite. Fillers may be added including coarse ground
limestone, fine ground limestone, clay, talc or other particulate fillers. The advantages of this invention and its operating
parameters will be further understood with reference to the following
detailed examples.
EXAMPLE 1
A cable jacket for use in power supply to electric
locomotives consisted of 1 00 parts chlorosulfonated polyethylene
elastomer (ASTM designation CSM, trade name Hypalon), 80 parts kaolin
clay, 20 parts carbon black, 30 parts trioctyl trimellitate plasticizer,
44 parts litharge stabilizer, and minor amounts of curatives. After
extrusion as a cable jacket, and vulcanization, this compound yielded
TCLP lead extraction of 90-100 mg/l. The TCLP analysis of 40 CFR 261
is incorporated herein in its entirety by reference.
EXAMPLE 2
The cable jacket of Example 1 was made employing the
same composition except that 22 parts of calcium phosphate were added
to the composition and, after extrusion as a cable jacket and
vulcanization, the product yielded TCLP lead extraction of 22 mg/l. Thus,
employing the metal phosphate of this invention in the haiogenated
polymer composition enabled the reduction of extractable lead from
90-1 00 mg/l to 22 mg/I.
EXAMPLE 3
The cable jacket of Example 1 was made and the identical
procedures were followed except that 44 parts of litharge were replaced with 25 parts of red lead. TCLP lead extraction of this cable jacket was
1 0 mg/l.
EXAMPLE 4
The procedure of Example 3 was repeated except that
1 2.5 parts of calcium phosphate was added to the formulation and, after
extrusion as a cable jacket and vulcanization, the product yielded TCLP
lead extraction of 3.6 mg/l. Thus, employing a metal phosphate of this
invention enabled the reduction of extractable lead from 1 0 mg/l to
3.6 mg/l.
EXAMPLE 5
Chloropolyethylene wire insulation product consisting of
1 00 parts chloropolyethylene, 60 parts clay, 40 parts calcium carbonate,
20 parts ester plasticizer, 1 2 parts litharge stabilizer, plus antioxidant and
cross linking agents was made. After extrusion and vulcanization, the
product yielded TCLP lead extraction values of 20-30 mg/l which is above
the limiting value of 5 mg/l needed for qualification as nonhazardous
waste.
EXAMPLE 6
The procedures of Example 5 were repeated except that
litharge was replaced with a preblended stabilizer containing 60% by
weight litharge and 40% by weight calcium phosphate (CaHP04) . The
product yielded TCLP lead extraction values of 2-3 mg/l, thereby
qualifying as nonhazardous waste. Thus, this invention enables the reduction of hazardous waste materials and greatly reduces the cost of
transportation to a suitable recycling site.
EXAMPLE 7
Dibasic lead phthalate was found to have an oral LD50 value
in rats of between 2000-5000 mg/kg body weight, placing it in
Category III (formerly known as Slightly Toxic). A blend of 67% dibasic
lead phthalate, 33% zinc phosphate, was found to have an oral LD50
value in rats of greater than 5000 mg/kg body weight, corresponding to
Category IV (formerly known as Nontoxic). It is not believed that any
lead stabilizer has previously been found to have an oral LD value above
5000 mg/kg. Accordingly, this invention offers the advantage of
producing nontoxic lead stabilizer systems. It has also been found that
the blends appear to be less soluble in digestive fluids which would
reduce the toxicity in animals where compositions containing lead
stabilizer components were ingested.
EXAMPLE 8
A composition was prepared comprising polyvinyl chloride
(PVC) 100 parts by wt., calcium carbonate 40, di-iso-decyl phthalate 65,
stearic acid 0.3, and tribasic lead sulfate 4. This composition is routinely
used as a nonmetallic (Underwriters Laboratories Type NM) jacket to
cover residential building wire. This composition was mixed to a
homogeneous state and extruded, simulating wire manufacture. The
composition yielded TCLP extraction of 7 mg/l. EXAMPLE 9
The composition of EXAMPLE 8 was mixed using a blend of
4 parts of tribasic lead sulfate with 2 parts of Na2HP04 in place of the
above 4 parts of pure tribasic lead sulfate. This composition yielded
TCLP extraction of 1 .5 mg/l.
The above data establishes that minor amounts of an alkali
or alkaline earth metal, Group II and Group lla metal phosphate, when
employed as an additive in haiogenated polymer compositions reduces
extractable lead, as a heavy metal, of the lead stabilizer employed in the
compositions. The above examples are not intended to limit the
invention. In accordance with the principles, other haiogenated polymers
that are stabilized with heavy metals may be landfillable as
non-hazardous waste by adding an effective quantity of the metal
phosphate to pass the TCLP as provided in 40 CFR 261 .
Having described this invention, its advantages and
operating parameters, it will be obvious to persons of ordinary skill in the
art, in view of the above description, that variations hereof may be made
without departing from the spirit and scope thereof.
WHAT IS CLAIMED IS:

Claims

1 . A haiogenated polymer composition comprising a
haiogenated polymer, a heavy metal compound stabilizer for said polymer
and a metal phosphate as an additive in an effective amount to reduce
extraction of heavy metal when said composition is exposed to the
toxicity characteristic leaching procedure of 40 CFR 261 .
2. The composition of claim 1 wherein said haiogenated
polymer is selected from the group of polyvinyl chloride, polychloroprene,
chlorinated polyethylene and chlorosulfonated polyethylene.
3. The composition of claim 1 wherein said metal phosphate is
calcium phosphate.
4. The composition of claim 1 wherein said heavy metal
compound is selected from the group consisting of litharge, red lead,
dibasic lead phthalate, dibasic lead phosphite, tribasic lead sulfate,
tetrabasic lead sulfate, tribasic lead maleate, tetrabasic lead fumarate,
basic lead carbonate and dibasic lead stearate.
5. The composition of claim 1 wherein said heavy metal
compound stabilizer is present in an amount from about 0.5 to about
40 parts and said metal phosphate is present in an amount from 0.2 to
about 20 parts and said haiogenated polymer is present in amount of
about 1 00 parts.
6. The composition of claim 1 wherein the metal phosphate is
selected from the group consisting of an alkali metal phosphate and an
alkaline earth metal phosphate.
7. A haiogenated polymer composition comprising a polymer or
copolymer of vinyl chloride, a lead stabilizer selected from the group
consisting of litharge, red lead, dibasic lead phthalate, dibasic lead
phosphite, tribasic lead sulfate, tetrabasic lead sulfate, tribasic lead
i maleate, tetrabasic lead fumarate, basic lead carbonate and dibasic lead
stearate, and a metal phosphate as an additive in an effective amount to
reduce extraction of the lead when said composition is exposed to the
toxicity characteristic leaching procedure of 40 CFR 261 .
8. The composition of claim 7 wherein the metal phosphate has
a metal cation selected from the group consisting of calcium, magnesium,
strontium, barium and zinc.
9. The composition of claim 7 wherein said metal phosphate is
in an amount of about 0.2 to about 20 parts and the lead compound is
in an amount of about 0.5 to about 40 parts per 1 00 parts resin.
10. The composition of claim 7 wherein said metal phosphate is
calcium phosphate.
1 1 . A method for reducing extractable heavy metal from a
molded product of a haiogenated polymer composition comprising
providing a haiogenated polymer composition containing a
heavy metal compound stabilizer for said polymer to produce a molded
product,
adding a metal phosphate as an additive in an effective
amount to reduce extraction of the lead when said molded product is
exposed to the toxicity characteristic leaching procedure 40 CFR 261 .
1 2. The method of claim 1 1 wherein said heavy metal compound
is selected from the group consisting of litharge, red lead, dibasic lead
phthalate, dibasic lead phosphite, tribasic lead sulfate, tetrabasic lead
sulfate, tribasic lead maleate, tetrabasic lead fumarate, basic lead
carbonate and dibasic lead stearate, and a metal phosphate as an additive
in an effective amount to reduce extraction of the lead when said
composition is exposed to the toxicity characteristic leaching procedure
of 40 CFR 261 .
1 3. The method of claim 1 1 wherein said heavy metal stabilizer
is present in an amount from about 0.5 to about 40 parts and said metal
phosphate is present in an amount from 0.2 to about 20 parts and said
haiogenated polymer is present in an amount of about 1 00 parts.
14. The method of claim 1 3 wherein said metal phosphate is
calcium phosphate.
1 5. The method of claim 1 2 wherein the metal phosphate is
selected from the group consisting of calcium, magnesium, strontium,
barium and zinc.
PCT/US1999/010660 1998-05-15 1999-05-14 Method for reducing extractable heavy metals (lead) from halogenated polymer compositions WO1999060055A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU39909/99A AU3990999A (en) 1998-05-15 1999-05-14 Method for reducing extractable heavy metals (lead) from halogenated polymer compositions

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US7971298A 1998-05-15 1998-05-15
US09/079,712 1998-05-15

Publications (1)

Publication Number Publication Date
WO1999060055A1 true WO1999060055A1 (en) 1999-11-25

Family

ID=22152313

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US1999/010660 WO1999060055A1 (en) 1998-05-15 1999-05-14 Method for reducing extractable heavy metals (lead) from halogenated polymer compositions

Country Status (2)

Country Link
AU (1) AU3990999A (en)
WO (1) WO1999060055A1 (en)

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1339429A (en) * 1969-12-18 1973-12-05 Mitsubishi Plastics Ind Polyvinyl chloride conduits and utensils
US4670494A (en) * 1985-07-30 1987-06-02 Gary Chemical Corp. Flame retardant low smoke poly(vinyl chloride) thermoplastic composition
US4892683A (en) * 1988-05-20 1990-01-09 Gary Chemical Corporation Flame retardant low smoke poly(vinyl chloride) thermoplastic compositions
WO1990003999A1 (en) * 1988-10-07 1990-04-19 M&T Chemicals Inc. Improved stabilizers for halogen-containing polymers
US5227417A (en) * 1992-01-24 1993-07-13 Cooper Industries, Inc. Polyvinyl chloride based plenum cable
US5270366A (en) * 1992-12-16 1993-12-14 Vista Chemical Company Lead stabilized, flexible polymeric blends containing polyvinylchloride

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1339429A (en) * 1969-12-18 1973-12-05 Mitsubishi Plastics Ind Polyvinyl chloride conduits and utensils
US4670494A (en) * 1985-07-30 1987-06-02 Gary Chemical Corp. Flame retardant low smoke poly(vinyl chloride) thermoplastic composition
US4892683A (en) * 1988-05-20 1990-01-09 Gary Chemical Corporation Flame retardant low smoke poly(vinyl chloride) thermoplastic compositions
WO1990003999A1 (en) * 1988-10-07 1990-04-19 M&T Chemicals Inc. Improved stabilizers for halogen-containing polymers
US5227417A (en) * 1992-01-24 1993-07-13 Cooper Industries, Inc. Polyvinyl chloride based plenum cable
US5270366A (en) * 1992-12-16 1993-12-14 Vista Chemical Company Lead stabilized, flexible polymeric blends containing polyvinylchloride

Also Published As

Publication number Publication date
AU3990999A (en) 1999-12-06

Similar Documents

Publication Publication Date Title
KR100644490B1 (en) Flame retardant composition for cable covering material and ocean cable using the same
EP0393813B1 (en) Flame retardant and a flame-retardant resin composition containing the same
EP0280761A2 (en) Flame-retardant olefinic resin composition
AU2017421247A1 (en) Flame retardant, low smoke, cold resistant electric cable
EP1059330A1 (en) Halogen-free flame-retardant resin composition
KR101571104B1 (en) Flame-Retardant Insulating Composition Resistant to Heat and Radiation and Electrical Cable Produced with the Same
US4327001A (en) Low smoke polyolefin jacket composition for electrical wire
CA1221188A (en) Flame retardant crosslinked ethylene copolymer electrical insulation
Brown Compounding of ethylene-propylene polymers for electrical applications
US5475045A (en) Method and composition for reducing extractable heavy metals from vinyl halide resin compositions
JP3723025B2 (en) Non-halogen flame retardant resin composition
WO1999060055A1 (en) Method for reducing extractable heavy metals (lead) from halogenated polymer compositions
JP2000191844A (en) Non-halogen flame retardant resin composition
US5439742A (en) Electrical insulating vinyl halide resin compositions
JP2000290438A (en) Nonhalogen flame retardant resin composition and flame retardant electric wire and cable using the same
JP3193017B2 (en) Non-halogen flame-retardant resin composition
JP2007246572A (en) Non-halogenous resin composition and electric wire and cable which are covered by the resin composition
WO2001036530A1 (en) Smoke and fire retardant plenum compositions
EP1461381A1 (en) Stability improvement of aluminium hydroxide in pvc compound
KR840001713B1 (en) Compositions of alkylen-alhyl a crylate copolymers having improved flame retandant properties
JPH07173339A (en) Cross-linkable highly flame retardant composition
GB2185262A (en) Polyolefin composition
JPS62252442A (en) Abrasion-resistant flame-retarding composition
JP2000191841A (en) Non-halogen flame retardant resin composition
JP2000251538A (en) Non-halogen incombustible resin composition

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AE AL AM AT AU AZ BA BB BG BR BY CA CH CN CU CZ DE DK 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 MD MG MK MN MW MX NO NZ PL PT RO RU SD SE SG SI SK SL TJ TM TR TT UA UG UZ VN YU ZA ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): GH GM KE LS MW SD SL SZ UG 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 BF BJ CF CG CI CM GA GN GW ML MR NE SN TD TG

NENP Non-entry into the national phase

Ref country code: KR

121 Ep: the epo has been informed by wipo that ep was designated in this application
REG Reference to national code

Ref country code: DE

Ref legal event code: 8642

122 Ep: pct application non-entry in european phase