CA2208602C - Intumescent putty - Google Patents
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- CA2208602C CA2208602C CA002208602A CA2208602A CA2208602C CA 2208602 C CA2208602 C CA 2208602C CA 002208602 A CA002208602 A CA 002208602A CA 2208602 A CA2208602 A CA 2208602A CA 2208602 C CA2208602 C CA 2208602C
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Abstract
This invention relates to non-aqueous, indefinitely conformable, halogen free, intumescent putty useful in an opening as a firestop material to deter the spread of fire, smoke, and vapors during a fire.
Description
INTUMESCENT PUTTY
Field of the Invention This invention relates too intumescent putty for use in an opening as a firestop material to deter the spread of flame, smoke, and vapors during a fire.
Description of Related Art Firestop products are u:~ed to reduce or eliminate the chimney effect at through-penetrations. Characteristics of firestop materials suitable for typical commercial uses include the ability to expand and to char. Further, the charred material preferably has sufficient strength to withstand a hose stream test.
An industry recognized fire endurance test used to evaluate firestop materials is the American Society of Testing Materials' test identified as "ASTM E-814-83". This test includes subjecting the charred material to a stream of water from a fire hose.
US-A-5,025,058 describes a flame-resistant non-drying putty composition where the chief ingredients are an unvulcanized rubber, intumescent material such as a metal hydrate and liquid chloroprene as a liquid polymer resin.
JP-A-57-209980 relates to a putty composition containing a liquid polychloropren.e as a key ingredient, hydrated alumina as intumescent material and silicone rubber.
GB-A-2 092 599 describes a fireproof putty composition containing liquid chloroprene and a specific unvulcanized chloroprene rubber with intumescent material.
Summary of the Invention According to one aspect of the present invention, there is provided an intumescent putty that remains soft and.
handleable for at least a month under ambient conditions comprising a blend of intumescent material, vulcanized rubber, and unvulcanized rubber, said vulcanized rubber and said unvulcanized rubber together providing said putty with a softness value of at least 4 mm,, wherein measurement of the softness of the putty is described in ASTM D-1403-91, containing less than 0.25 percent by weight halogen, said putty containing less than 0.25 percent by weight water other than bound water, wherein bound water is water that does not come off until the putty is heated to at least 100°C, and said putty containing less than 0.25 percent by weight rubber curing agent, based on the total weight of the putty.
The present invention provides a non-aqueous, indefinitely conformable, halogen-free, intumescent putty comprising a blend of intumescent material, rubber, and unvulcanized rubber, the rubber and unvulcanized rubber together provide the putty with a softness value of at least 4 mm (preferably, at least 9:.5 mm; more preferably at least 5 mm; and even more preferably, at least 6 mm).
Further, the putty is la essentially free (i.e., contains less than 0.25 percent by weight) of a rubber curing agent.
In another aspect, the present invention provides a non-aqueous, indefinitely conformable, halogen-free, intumescent putty comprising a blend of intumescent to material, rubber, and at least 5 percent (preferably, , at least 10 percent: more preferably, at least 15 percent) by weight unvulcanized rubber, based on the total weight of the putty. The putty has a softness value of at least 4 mm (preferably, at least 4.5 mm~
more preferably at least 5 mm~ and even more preferably, at least 6 mm) and is essentially free of a rubber curing agent.
Preferably, the rubber is selected from the group consisting of natural rubber, butyl rubbers, 2o polybutadiene rubbers, synthetic isoprene rubbers, styrene butadiene rubbers, ethylene acrylic rubbers, nitrile rubbers, urethane rubbers, ethylene vinyl acetate rubbers, and combinations thereof. Preferably, the unvulcanized rubber is selected from the group consisting of unvulcanized natural rubber, unvulcanized butyl rubbers, unvulcanized polybutadiene rubbers, unvulcanized synthetic isoprene rubbers, unvulcanized styrene butadiene rubbers, unvulcanized ethylene acrylic rubbers, unvulcanized nitrile rubbers, unvulcanized urethane rubbers, unvulcanized ethylene vinyl acetate rubbers, and combinations thereof.
Optionally, the intumescent putty according to the invention further comprises one or more of a plasticizes, a flame retardant, a char former, a filler, a colorant, a wax, an antioxidant, and/or an ' antiozonant.
Field of the Invention This invention relates too intumescent putty for use in an opening as a firestop material to deter the spread of flame, smoke, and vapors during a fire.
Description of Related Art Firestop products are u:~ed to reduce or eliminate the chimney effect at through-penetrations. Characteristics of firestop materials suitable for typical commercial uses include the ability to expand and to char. Further, the charred material preferably has sufficient strength to withstand a hose stream test.
An industry recognized fire endurance test used to evaluate firestop materials is the American Society of Testing Materials' test identified as "ASTM E-814-83". This test includes subjecting the charred material to a stream of water from a fire hose.
US-A-5,025,058 describes a flame-resistant non-drying putty composition where the chief ingredients are an unvulcanized rubber, intumescent material such as a metal hydrate and liquid chloroprene as a liquid polymer resin.
JP-A-57-209980 relates to a putty composition containing a liquid polychloropren.e as a key ingredient, hydrated alumina as intumescent material and silicone rubber.
GB-A-2 092 599 describes a fireproof putty composition containing liquid chloroprene and a specific unvulcanized chloroprene rubber with intumescent material.
Summary of the Invention According to one aspect of the present invention, there is provided an intumescent putty that remains soft and.
handleable for at least a month under ambient conditions comprising a blend of intumescent material, vulcanized rubber, and unvulcanized rubber, said vulcanized rubber and said unvulcanized rubber together providing said putty with a softness value of at least 4 mm,, wherein measurement of the softness of the putty is described in ASTM D-1403-91, containing less than 0.25 percent by weight halogen, said putty containing less than 0.25 percent by weight water other than bound water, wherein bound water is water that does not come off until the putty is heated to at least 100°C, and said putty containing less than 0.25 percent by weight rubber curing agent, based on the total weight of the putty.
The present invention provides a non-aqueous, indefinitely conformable, halogen-free, intumescent putty comprising a blend of intumescent material, rubber, and unvulcanized rubber, the rubber and unvulcanized rubber together provide the putty with a softness value of at least 4 mm (preferably, at least 9:.5 mm; more preferably at least 5 mm; and even more preferably, at least 6 mm).
Further, the putty is la essentially free (i.e., contains less than 0.25 percent by weight) of a rubber curing agent.
In another aspect, the present invention provides a non-aqueous, indefinitely conformable, halogen-free, intumescent putty comprising a blend of intumescent to material, rubber, and at least 5 percent (preferably, , at least 10 percent: more preferably, at least 15 percent) by weight unvulcanized rubber, based on the total weight of the putty. The putty has a softness value of at least 4 mm (preferably, at least 4.5 mm~
more preferably at least 5 mm~ and even more preferably, at least 6 mm) and is essentially free of a rubber curing agent.
Preferably, the rubber is selected from the group consisting of natural rubber, butyl rubbers, 2o polybutadiene rubbers, synthetic isoprene rubbers, styrene butadiene rubbers, ethylene acrylic rubbers, nitrile rubbers, urethane rubbers, ethylene vinyl acetate rubbers, and combinations thereof. Preferably, the unvulcanized rubber is selected from the group consisting of unvulcanized natural rubber, unvulcanized butyl rubbers, unvulcanized polybutadiene rubbers, unvulcanized synthetic isoprene rubbers, unvulcanized styrene butadiene rubbers, unvulcanized ethylene acrylic rubbers, unvulcanized nitrile rubbers, unvulcanized urethane rubbers, unvulcanized ethylene vinyl acetate rubbers, and combinations thereof.
Optionally, the intumescent putty according to the invention further comprises one or more of a plasticizes, a flame retardant, a char former, a filler, a colorant, a wax, an antioxidant, and/or an ' antiozonant.
In this application:
"putty" refers to a cohesive, moldable material that does not substantially flow at ambient temperatures (typically temperatures in the range from about 0°C to about 50°C) ;
- l0 "indefinitely conformable" means the putty remains soft and handleable for at least one month, (preferably, one year; more preferably, at least five years; even more preferably, at least ten years; and most preferably, at least twenty years) under ambient temperatures (typically temperatures in the range from about 0°C to about 50°C) ;
"halogen-free" means essentially free of halogens (i.e., contains less than 0.25 percent (preferably, less than 0.1 percent; more preferably, less than 0.01 percent) by weight halogen calculated on an elemental basis as C1, F, etc., based on the total weight of the putty;
"non-aqueous" means essentially free of (i.e., contains less than 0.25 percent by weight) water, other than bound water, wherein bound water is water that does not come off until the material is heated to at least 100°C (preferably, at least 150°C, more preferably, at least 250°C) ;
"intumescent" refers to a material which expands 3o upon heating above about 100°C, although the temperature at which a particular intumescent material intumesces is dependent on the composition of that material;
"intumescent putty" refers to a putty that intumeces to at least two times (preferably at least three times) its (original) unexpanded volume (i.e., " its volume prior to intumescing);
"putty" refers to a cohesive, moldable material that does not substantially flow at ambient temperatures (typically temperatures in the range from about 0°C to about 50°C) ;
- l0 "indefinitely conformable" means the putty remains soft and handleable for at least one month, (preferably, one year; more preferably, at least five years; even more preferably, at least ten years; and most preferably, at least twenty years) under ambient temperatures (typically temperatures in the range from about 0°C to about 50°C) ;
"halogen-free" means essentially free of halogens (i.e., contains less than 0.25 percent (preferably, less than 0.1 percent; more preferably, less than 0.01 percent) by weight halogen calculated on an elemental basis as C1, F, etc., based on the total weight of the putty;
"non-aqueous" means essentially free of (i.e., contains less than 0.25 percent by weight) water, other than bound water, wherein bound water is water that does not come off until the material is heated to at least 100°C (preferably, at least 150°C, more preferably, at least 250°C) ;
"intumescent" refers to a material which expands 3o upon heating above about 100°C, although the temperature at which a particular intumescent material intumesces is dependent on the composition of that material;
"intumescent putty" refers to a putty that intumeces to at least two times (preferably at least three times) its (original) unexpanded volume (i.e., " its volume prior to intumescing);
"rubber" refers to materials including natural rubber and synthetic rubbers (or synthetic elastomers) that exhibit stretch and recovery after being cured (or vulcanized):
"unvulcanized rubber" refers to the precursor to material that when vulcanized (or cured) provides rubber:
"rubber curing agent" refers to a vulcanizing, curing, or crosslinking agent such as sulfur, amines, or difunctional acids, divinyl benzene, or a free radical initiator such as dicumyl peroxide which when compounded and activated with the unvulcanized rubber produces rubber wherein the cure conditions and concentration of agents) and/or free radical initiators) determine the extent of vulcanization "softness value" is a measure of the softness of the putty and is determined as described below under the heading "Softness Value Measurement":
"softness" refers to the ability of the putty to be shaped or molded by hand with ease:
"moldable" means the putty is conformable (e. g., the putty can be wrapped around a pipe);
"cohesion" means that the putty adheres to itself and, once molded, retains its shape until acted upon by an external force:
"adhesion" refers to the ability of the putty to adhere to a dissimilar material (i.e., the putty has sufficient tack to stay in place when molded around construction components (e. g., concrete, dry wall, metal, plastic, and cables)), but not so much tack that it adheres to skin: "
"reusable" refers to the ability of the putty installed in one location to be removed and installed "
in another location, without substantially affecting the intumescence, softness, and flame retardance properties of the putty and "char strength" is a measure of the strength of the expanded carbonaceous residue ("char") formed from the putty after exposure to temperatures above about l0 350°C for about 15 minutes.
Intumescent putties according to the present invention typically are reuseable, exhibit good adhesion properties, and can be used to restore acceptable fire ratings of floors and walls after penetrations (or openings) are made in them. Such penetrations are made, for example, to accommodate the passage of cables, conduits, metal and plastic pipe, and telephone installations. If the penetrations or openings around the installations that pass through the 2o penetrations are not adequately sealed, flame, smoke, and/or water may pass there through and extend the destruction of a fire and/or water damage.
Description of Preferred Embodiments The intumescent putty according to the present invention remains in a soft, pliable, and unexpended condition until it is exposed to heat at temperatures in excess of about 100°C (212°F). When heated above about 350°C (662°F), the putty readily intumesces typically to about three times its original volume, and begins to form char that further enhances the putty's flame retardant characteristics. The putty seals voids in through-penetrations caused by burning and/or melting materials, effectively preventing the passage of flame, smoke, vapors, and water from one location (e. g., a room or floor) to another.
"unvulcanized rubber" refers to the precursor to material that when vulcanized (or cured) provides rubber:
"rubber curing agent" refers to a vulcanizing, curing, or crosslinking agent such as sulfur, amines, or difunctional acids, divinyl benzene, or a free radical initiator such as dicumyl peroxide which when compounded and activated with the unvulcanized rubber produces rubber wherein the cure conditions and concentration of agents) and/or free radical initiators) determine the extent of vulcanization "softness value" is a measure of the softness of the putty and is determined as described below under the heading "Softness Value Measurement":
"softness" refers to the ability of the putty to be shaped or molded by hand with ease:
"moldable" means the putty is conformable (e. g., the putty can be wrapped around a pipe);
"cohesion" means that the putty adheres to itself and, once molded, retains its shape until acted upon by an external force:
"adhesion" refers to the ability of the putty to adhere to a dissimilar material (i.e., the putty has sufficient tack to stay in place when molded around construction components (e. g., concrete, dry wall, metal, plastic, and cables)), but not so much tack that it adheres to skin: "
"reusable" refers to the ability of the putty installed in one location to be removed and installed "
in another location, without substantially affecting the intumescence, softness, and flame retardance properties of the putty and "char strength" is a measure of the strength of the expanded carbonaceous residue ("char") formed from the putty after exposure to temperatures above about l0 350°C for about 15 minutes.
Intumescent putties according to the present invention typically are reuseable, exhibit good adhesion properties, and can be used to restore acceptable fire ratings of floors and walls after penetrations (or openings) are made in them. Such penetrations are made, for example, to accommodate the passage of cables, conduits, metal and plastic pipe, and telephone installations. If the penetrations or openings around the installations that pass through the 2o penetrations are not adequately sealed, flame, smoke, and/or water may pass there through and extend the destruction of a fire and/or water damage.
Description of Preferred Embodiments The intumescent putty according to the present invention remains in a soft, pliable, and unexpended condition until it is exposed to heat at temperatures in excess of about 100°C (212°F). When heated above about 350°C (662°F), the putty readily intumesces typically to about three times its original volume, and begins to form char that further enhances the putty's flame retardant characteristics. The putty seals voids in through-penetrations caused by burning and/or melting materials, effectively preventing the passage of flame, smoke, vapors, and water from one location (e. g., a room or floor) to another.
In another aspect, the putty according to the present invention typically resists flow when subjected to heat. This resistance to flow allows the putty to remain intact at elevated temperatures (i.e., temperatures normally encountered during combustion).
to If the temperature rises sufficiently (i.e., under the .
conditions of a fire) the putty may char as well as intumesce.
The general effect of the amounts of materials used to prepare a particular putty according to the present invention on properties such as softness and resistance to flow should be apparent to one skilled in the art after review of the disclosure herein.
Preferably, the putty comprises in the range from about 5 to about 50 percent (preferably, about 15 to about 30 percent) by weight rubber and unvulcanized rubber, based on the total weight of the putty.
In another aspect, the putty preferably comprises in the range from about 10 to about 50 percent (preferably, about 10 to about 25 percent) by weight unvulcanized rubber, based on the total weight of the putty.
In another aspect, the putty preferably comprises in the range from about 1 to about 15 percent (preferably, about 2 to about 8 percent) by weight rubber, based on the total weight of the putty.
The putty can be made by, and is typically made by a method that includes compounding rubber and unvulcanized rubber. Although not wanting to be bound by theory, it is believed that the rubber and the unvulcanized rubber provide a balance between softness and conformability and flow resistance at elevated temperatures.
to If the temperature rises sufficiently (i.e., under the .
conditions of a fire) the putty may char as well as intumesce.
The general effect of the amounts of materials used to prepare a particular putty according to the present invention on properties such as softness and resistance to flow should be apparent to one skilled in the art after review of the disclosure herein.
Preferably, the putty comprises in the range from about 5 to about 50 percent (preferably, about 15 to about 30 percent) by weight rubber and unvulcanized rubber, based on the total weight of the putty.
In another aspect, the putty preferably comprises in the range from about 10 to about 50 percent (preferably, about 10 to about 25 percent) by weight unvulcanized rubber, based on the total weight of the putty.
In another aspect, the putty preferably comprises in the range from about 1 to about 15 percent (preferably, about 2 to about 8 percent) by weight rubber, based on the total weight of the putty.
The putty can be made by, and is typically made by a method that includes compounding rubber and unvulcanized rubber. Although not wanting to be bound by theory, it is believed that the rubber and the unvulcanized rubber provide a balance between softness and conformability and flow resistance at elevated temperatures.
s A preferred rubber is a styrene butadiene rubber, characterized by the manufacturer as having a high degree of crosslinking (commercially available under TM
the trade designation "POLYSAR S1018" from Polysar Rubber Div. of Miles, Inc.). A styrene butadiene 1o rubber, characterized by the manufacturer as having a low Mooney viscosity (commercially available from Ameripol Synpol Co., a Division of Uniroyal GoodrYch Tire Co. of Akron, OH) is the preferred unvulcanized rubber. _ is In a preferred embodiment two types of rubbers are used together with an unvulcanized rubber. The first rubber is preferably a styrene butadiene rubber, characterized by the manufacturer as having a high degree of crosslinking ("POLYSAR 51018"j. The amount 20 of this rubber preferably ranges from about 10 to about 40 percent by weight of the total rubber and unvulcanized rubber content of the putty. The second rubber is preferably a butyl rubber characterized by the manufacturer as "moderately" crossliriked"
2s (commercially available under the trade designation TM
"POLYSAR BUTYL XL 68102" from Polysar Rubber Div. of Miles, Inc. of Akron, OH). This second rubber is' believed to provide a desirable level of stretch.
Preferably, the amount of this rubber ranges from about 30 1 percent by weight to about 5 percent (more preferably, about 1 to about 2 percent) by weight of the total rubber and unvulcanized rubber content of the putty. If the amount of moderately crosslinked rubber is greater than about 5 percent by weight, the material 35 tends to be undesirably tacky, and may be difficult to install in some applications. At levels of less than 1 percent by weight, typically no benefit in stretch is observed from its addition to the formulation.
the trade designation "POLYSAR S1018" from Polysar Rubber Div. of Miles, Inc.). A styrene butadiene 1o rubber, characterized by the manufacturer as having a low Mooney viscosity (commercially available from Ameripol Synpol Co., a Division of Uniroyal GoodrYch Tire Co. of Akron, OH) is the preferred unvulcanized rubber. _ is In a preferred embodiment two types of rubbers are used together with an unvulcanized rubber. The first rubber is preferably a styrene butadiene rubber, characterized by the manufacturer as having a high degree of crosslinking ("POLYSAR 51018"j. The amount 20 of this rubber preferably ranges from about 10 to about 40 percent by weight of the total rubber and unvulcanized rubber content of the putty. The second rubber is preferably a butyl rubber characterized by the manufacturer as "moderately" crossliriked"
2s (commercially available under the trade designation TM
"POLYSAR BUTYL XL 68102" from Polysar Rubber Div. of Miles, Inc. of Akron, OH). This second rubber is' believed to provide a desirable level of stretch.
Preferably, the amount of this rubber ranges from about 30 1 percent by weight to about 5 percent (more preferably, about 1 to about 2 percent) by weight of the total rubber and unvulcanized rubber content of the putty. If the amount of moderately crosslinked rubber is greater than about 5 percent by weight, the material 35 tends to be undesirably tacky, and may be difficult to install in some applications. At levels of less than 1 percent by weight, typically no benefit in stretch is observed from its addition to the formulation.
WO 96/20987 PCTJUS9~/16633 Suitable intumescent materials include hydrated alkali metal silicates (e. g., sodium silicate, lithium silicate, and potassium silicate with bound water), expandable graphite, unexpanded vermiculite, and organic intumescent compounds such as melamine (i.e., l0 2, 4, 6-triamino-1, 3, 5-triazine), azocarbonamide, and ~
benzene sulfonyl hydrazide which decompose to give off gases. The amount of intumescent material in the formulation varies depending on the type of intumescent chosen.
The preferred intumescent material is a granular hydrated alkali metal silicate intumescent composition comprising a mixture of bound water; at least one alkali metal silicate having the formula MZO:xSi02 (e. g., sodium silicate, lithium silicate, and potassium silicate), wherein M is an alkali metal and x ranges from about 1.5 to about 4, and at least one oxy boron compound selected from the group consisting of boric acid and borate salts of group I and II elements (e. g., metaborate, tetraborate, perborate, polyborate radicals, boric acid, colemanite, calcium metaborate, magnesium borate, and zinc borate) (see, e.g., U.S.
Pat. No. 4,521,333 (Graham, et al.).
Preferably, the molar ratio of boron (present in the oxy boron compound) to M is between about 0.2 and about 0.9. The water preferably comprises about 5 to 15 percent by weight of the mixture of water, oxy boron compound(s), and alkali metal silicate(s).
Preferably, the intumescent material is added in particulate form to the rubber and unvulcanized rubber in an amount sufficient to allow the putty to pass the fire test described below under the heading "Flame Through Test," but not so much that it makes the putty non-pliable, or that it adversely affects the char that forms in a fire such that heated putty does not pass the Fire Hose Stream Test described below.
Typically, the amount o.E intumescent material (e. g. hydrated alkali metal silicate) used ranges from about 50 to about 200 percent (preferab:Ly about 100 to about 140 percent) by weight of the total vulcanized rubber and unvulcanized rubber content of thES putty. In another aspect, the hydrated alkali metal silicate preferable is present in the range from about 5 to about 45 percent by weight, based on the total weight of the putty.
The hydrated alkali metal silicate particles typically range in size from about 75 micrometers to about 500 micrometers.
A silicate intumescent material such as hydrated sodium silicate is preferably used together with a silicate fluxing agent such as boric oxide. Such fluxing agents are used to stabilize the char formed when the putty is subjected to heat. A preferred silicate fluxing agent is anhydrous boric oxide (B203) , commf~rcially available from U.S. Borax of Valencia, CA. Boric: oxide can function as both a flame retardant and a silicate fluxing agent.
If the intumescent material is intercalated graphite, the putty preferably comprises in the range from about 5 to about 30 percent by weight intumescent material, based on the total weight of the putty.
It is within the scope of the present invention to use combinations of intumescent material (e. g., to use both hydrated alkali metal silicate and intercalated graphite).
Preferably, a sufficient amount of plasticizer is included in the putty to obtain the desired level of softness and moldability. Plasticizers are compounds that increase the flexibility of a material and facilitate processing. Suitable plasticizers include 9a s aromatic oils, naphthenic oils, mineral oil, waxes, phthalate esters such as dioctyl phthalate (DOP) or dibutyl phthalate, and phosphate esters such as 2-ethylhexyl diphenyl phosphate (commercially available, for example, under the trade designation '"SANITIZER
141"' from Monsanto of St. Louis, MO), isodecyl diphenyl phosphate, or triaryl phosphate ester (commercially available, for example, under the trade designation TM
"SANITIZ~R 143"' from Monsanto). A preferred plasticizes is isobutylene/butene copolymer liquid 1s commercially available under the trade designation °INDOPOL H100" from Amoco Oil Co. of Chicago, IL.
Suitable waxes include petrolatum (commercially available, for example, under the trade designations' "6916 WA7CM~ and '"PAXWAX 5324~ from National Wax Division TM
of Dussek Campbell, Inc., Skokie, ~ IL: "'SR-172"' from .C.
TM
P. Hall Co. of Chicago, IL: and '"P~TROLATUM RP8"' from Witco Chemical Corp. of New York, NY).
Typically, the plasticizes is present in the range from about 30 to about 50 percent by weight (preferably, from about 35 to about 45 percent by weight, based on the total rubber and unvulcanized rubber content of the putty. In another aspect, the plasticizes typically is present, in the range from about 2 to about 25 percent by weight, based on the .
3o total weight of the putty.
Other optional ingredients that can be included in the putty formulation include flame retardants, char formers (e.g., char forming resins), fillers, colorants, antioxidants, and antiozonants.
3s Useful flame retardants include boric oxide: zinc borate: alumina trihydrate: nitrogen phosphates such as ethylene diamine phosphate (commercially available, for TM
example, under the trade designation '~AMGUARD ~DiAP"
~ 60557-5540 from Allright & Wilson Ltd. of Richmond, VA), dimelamine phosphate (commercially available, for example, under the trade designation ~AMGUARD ND"' from Allright & Wilson Ltd.), melamine phosphate (commercially available, for example, under the trade TM
to designation '"AMGUARD NH"' from Allright 6 Wilson Ltd. ) , ammonium polyphosphate (commercially available, for TM
example, under the trade designations "PHOS CHEK'P30"' TM
and "PROS CHEK P40~ from Monsan~o)~ and a blend of bis melaminium pentate and polyhedric oxide (commercially available, for example, under the trade designation TM
"CHAR GUARD 329" from Great Lakes Chemical Corp. of West Lafayette, IN).
Useful char forming resins include epoxy resins, phenolic resins, polycarboimide resins, urea-2o fonaaldehyde resins, and melamine-formaldehyde resins.
The general term "phenolic" refers to phenol-formaldehyde resins as well as resins comprising other phenol-derived compounds and formaldehydes. A
preferred char forming resin is an epoxy resin commercially available under the trade designation "SCOTCHCRST SR 265"' from the 3M Company of St. Paul, MN.
Fillers can used to adjust the hardness of the putty (i.e., fillers typically make the putty stiffer or harder), act as reinforcement, or reduce cost.
Fillers include fumed silica, clay, fly ash, colorants, perlite, venaiculite, inorganic fibers (e. g., glass fibers and mineral fibers), and organic fibers.
Melamine, which as discussed above is an organic intumescent material, is also useful as a filler to adjust the tack of the putty. A preferred filler is milled glass fiber (commercially available as "731ED
TM
FIBERGLAS" from Owens-Corning Fiberglas Corp. of ~ 60557-5540 S Toledo, OH), or chopped fiberglass fibers (commercially available, for example, under the trade designation ~799AB"' from Owens-Coming Fiberglas Corp. of Toledo, OH ) .
Colorants ( a . g . , iron oxide such as FeaO, or FeZ03 D
1o are useful for product' identification.
Antioxidants are compounds added to rubbers to protect the rubber against degradation by oxygen. Such compounds are typically comprised of aromatic amines.
Antiozonants may be used to protect the putty from 15 degradation by ozone. Some compounds may perform as antioxidants as well as antiozonants. A preferred antioxidant is thiodiethylene bis-(3,5-di-tert-butyl-9-hydroxy) hydrocinnamate (commercially available under r", .
the trade designation "IRGANOX 1035" from the Additives 2o Division of Ciba-Geigy Corp. of Hawthorne, NY).
A preferred antiozonant is a mixture of diaryl p-phenylene diamines (commercially available under the trade designation "WINGSTAY 100" from Goodyear Chemicals Division of Goodyear Tire and Rubber Co. of 25 Akron, OH) .
The putty can be made, by combining the ingredients used to make the putty using conventional techniques known in the art. Typically, the putty is made by mixing the various ingredients using a mogul mixer 3o equipped with circulating cooling water. The cooling water minimizes the build up of heat resulting from exothermic reaction of the ingredients and/or the action of mixing blades, therby preventing the intumescent material from prematurely intumescing.
3s Preferably, the rubber and unvulcanized rubber are added to the mixing chamber and mixed until thoroughly blended. Any fillers, silicate fluxing agents, char forming resins. waxes, colorants, flame retardant, lx melamine, antioxidants, and antiozonants are then added while the mixing operation continues. Plasticizer is typically added and then mixed in for a few minutes.
The last ingredient added is usually the intumescent material. The putty is typically mixed until l0 homogeneous and smooth (i.e., not lumpy). After mixing, the putty is ready to use.
For many firestop applications, the putty is typically extruded into sheets or pads (usually about 0.635 cm (0.25 inch thick). The sheets or pads are cut to provide the desired size or shape for a particular application. For some applications, the putty is formed into sticks or rope.
Objects and advantages of this invention are further illustrated by the following examples, but the particular materials and amounts thereof recited in these examples, as well as other conditions and details, should not be construed to unduly limit this invention. All parts and percentages are by weight unless otherwise indicated.
Softness Value Measurement The softness of the putty is determined using a penetrometer (available as Model 73510 from Precision Instruments of Chicago, IL). Measurement of the 3o softness of the putty involves dropping a weighted cone-shaped object into the putty, and then measuring the distance the object penetrates the putty. The test procedure is described in ASTM D-1403-91, which is entitled "Standard Test Methods for Cone Penetration of Lubricating Grease Using One-Quarter and One-Half Scale Cone Equipment," wherein the penetration measurements were made using a stainless steel, quarter scale cone as specified in the ASTM test method.
Specifically, the softness value of the putty was determined by packing the putty into a tube open at each end such that the putty was flush with both ends of the tube. The packed cylinder was allowed to stand , at room temperature (about 23°C) for a minimum of 12 to hours before the softness value was determined. -The cone and the shaft connected thereto weighed 9.38_+0.025 grams. An additional 150 grams was added to the top of the shaft. The tip of the cone-shaped object was placed so it just touched the surface of the putty packed into cylinder. For each measurement, the shaft was released and the cone allowed to sink into the putty for 5 seconds. The distance the cone sank into the putty during the 5 seconds was recorded. The softness values reported for Examples 1, 2, and 20 are 2o based on an average of 2 measurements. The softness values reported for Examples 3-19 are based on an average of 10 measurements.
Putty Flow Measurement Putty was packed into a tube (2.5 cm diameters 2.5 cm long) open at each end such that it was flush with both ends of the tube. The packed tube was then laid on its curved side in an oven at 200°C for 30 minutes.
The amount of flow that occurred during the 30 minutes of heating was determined visually to be excellent (i.e., no flow), very good (i.e., slight flow), good (i.e., some flow, but material did not flow onto the surface on which the tube was placed in the oven), fair, or very bad (i.e., material flowed freely out of the tube and onto the surface on which the tube was placed in the oven).
Flame Through Test The Flame Through Test follows the procedure set forth in ASTM'(American Society for Testing Materials) Test '"E 819-83,"' entitled "Standard Test Method for Fire Tests of Through-Penetration Fire Stops".
to This test is used to evaluate the use of putty in a through-penetration tire application.
For this test, a poured concrete slab, 11.4 cm .(4.5 in) thick and approximately 30.5 cm (3 ft) square, was prepared. Four 10.2 cm (9 in) diameter circular openings were made in the slab. The openings were evenly spaced. A 2.5 cm (1 in)) thick mineral fiber insulation material (commercially available under the trade designation. "USG 114 FIRE SAFING" from US .
2o Gypsum of Chicago, IL) was firmly packed into each .
opening in the slab. The mineral fiber was recessed about 2.5 cm from the top surface of the concrete. The putty was packed into the opening flush with the top surface of the concrete. The thickness 'of the putty was about 2.5 cm. The concrete slab was placed on the top of a gas-fired furnace (commercially available from Armil C.F.S. of South Iiolland, IL). The mineral fibers faced the heat source (flame) of the furnace.
The time and temperature parameters outlined in Figure 1 of ASTM E 819-B3 were followed for the test.
The test was run for 3 hours. unless flame through occurred. Flame through is indicated by flames coming through the opening to the "cold" side of the concrete slab. If there is flame through in less than 3 hours, then the material tested is deemed to have failed the test. If the opening remained sealed for the.3 hours, then the fire stop is given a passing designation (referred in ASTM E 819-83 as having an "F" rating).
Fire Hose Stream Test If a fire stop employing the putty of one of the examples passed the "Flame Through Test," then the following test, which is described in ASTM E 814-83, l0 was conducted.
Immediately after the "Flame Through Test," the slab was removed from the furnace and placed vertically in a metal stand. From a distance of 6.1 meters (20 ft), a stream of water was propelled in a sweeping motion against the material in the opening of the concrete slab at a pressure of 0.21 MPa (30 lbs/in2 ).
To pass this test, the material sealing the through-penetration, after having been subjected to the heat from a fire thus producing a char, had to withstand the 2o hose stream and continue to seal the pipe for a period of 1.5 seconds per 0.09 square meter,(i.e., 1.5 seconds per square foot) of test structure. For example, a 0.84 m2 (9 ft2) assembly must withstand a hose stream for 13.5 seconds.
~ 60557-5540 The ingredients used for the examples are listed in Table 1, below.
Table 1 Iags~edibat Trades Desigiution loaroa of Ingradieat Uavulcaaised styrene'"AMERIP01. SYNPOb Ameripol Syapol butadiene rubber 8107'x" Co. Division bf Uairoyal Goodrich Tire ' Co., Akso~n, OH
Styrene butadiene '"POLYSAR S lOlB"''"~Polysar Rubber rubber ~ Division of ' Milan, Pittsburgh, PA
Moderately "POLYSAR BUTYL Xh Polysar Rubber ~
crosslinked butyl 68102'T~ Division of rubbez Idiles, Pittaburgh, PA
Mixture of diaryl '"wINGSTAY 100'T~ Goodyear .
p-pheaylene diamine Chemicals Division of Goodyear Tise and R~bbes Co,., Jv)cron, Thiodiethyleae bin-"IRGANOX 1035' .W dditivea (3,5-di-tert-butyl-~- Division of hydroxy) Ciba-Geigy hydrocianaaate Corp., Narrthorne, NY
Fumed silica "CAB-O-SIL M-5" ~ Cabot Corp., .
Tuscola, II.
Epoxy resin po~rder'"SCOTCHCAST SR-265'The 3M Company, St. Paul, 1~1 Pos~dered iron oxide"IRON OXIDE BF-95"' Bailey (Fe=0>> Fagineers, Iae., Fairfield, AL
Soroa trioxide powder"ANHYDROUS BORIC tl.S. Borax, ACID"' ~" Valencia, G
Melamine po~dtr "AFRO MEIJ~MINE" Cytec (-60 ~
mesh) Industries, west Peterson, NJ
Milled glass '"?3~ED FIBERGLASS Oweas-Corafag, filaments 1/e""""~ Fiberglas Corp., Toledo, OH
Table 1 Continued Milled glaaa . "MFX-ll- 8 IN Phoenix filaments Fiberglas, Inc., oakville, Ontario, Canadi Chopped fiberglass "799A8"'r' . Ovens-Corning ' fibers, 1.25.cm Fiberglas Corp., (0.5 inch) lon Toledo, OH
Isobutylene butane '"INDOPOL H-~100"'~Amoco Chemical c of r 1i d Co., Chica , Ib Copolyaer of isobutyl'"POLYSAR BUTYL. Polysar Rubber 301"' and isoprene Division of Miles Petrolatum '"6916 i~A7C"~" Nation: Wax .
Division of Dussek Campbell, Ine., Skokie, IL
Petrolatum '"PA)CWAX 532"'"" Natioat Wax Division of Dussek Campbell.
Inc.
Petrolatum "PEN~~ ~~"' ~" Peareco zproducts C.;
Peateco Division, ICarns Cit , PA
Petrolatum '"PETROLATUM RP$'"7"'Witco Chemical Corp., Nsw York, NY
Blend of bis "CHARGUARD 32g'"" Grsat Lakes melaminium pentate Chemical Corp., and polyhedric oxide West Lafayette, (flame retardant) Intercalated graphite"GRAPHITE TG 326"'x"UGR Carbon Co., , flake ~ Inc., Danbury, Granulated hydrated'"EXPANTROL ~811"'~The 3M Company sodium silicate Granulated hydrated"EXPANTROL 2"''". The 3M Company sodium silicate Hydrated zinc borate"FIREBRAKE Z8 FINE""U.S. Horax i n. 1 II~.n~ I
a 60557-5540 Examples 1 and 2 The ingredients for Examples 1 and 2 are listed in Table 2, below.
Table 2 llmonn! of Ingredients, pgit~
Zagrediea! Example 1 P~cample Unvulcanized atysene 76.50 76.50 butadiene rubber ("AI~RIPOI. SYNPOI.
B107"')1""
Styrene butadiene rubber 20.00 20.00 ("POhYSAR S 1018")1""
Moderately croaslinked yl 3.50 3.50 but rubber ('POLYSAR XI. ~"
68102"'~
Mixture of diaryl p-phenylene 2.00 2.00 diamine ("NINGSTAY 100")s Thiodiethylene bin-(3,5-di-tert- 2.00 2.00 butyl-4-hydroxy) hydrocinnamate ('"IRG~1NOX 1035")1'"
Fumed silica ('"CA8-O-SII. 13.00 13:00 M 5"'JTM
Epoxy resin powder ("SCOTCHCAST 15.00 15.00 8R 265")1""
Powdered iron oxide 5.00 5.00 (FeZO~) ("IRON OXIDE BF 95"')TM
Melamine powder ('"HERO 50.00 75.00 , MELAMINE"' ) r"' Boron Oxide 10.00 X0.00 (Anh roua) Milled glass filaments 30.00 30.00 ('"731ED
FI BERGIJ4SS" f"
Isobutylene butane copolysier X0.00 50.00 1i id ("INDOPOh H 100")TM
Petrolatum ('"6916 WAX"')' 60.00 60.00 Granulated hydrated.spdium 120.00 silicate ('"EXPANTROI.
481"')1'"
Intercalated graphite ?0.00 flake ("GRAPHITE TG 326"')r'"
* Parts per hundred based on the total rubber sad unvulcanized rubber content of the putty.
The ingredients for each example were compounded ,15 using an internal mixer (Prep Mixer, Part # 02-2~-000, 350/420 cm' capacity: available from C. W. Hrabender Instruments, Inc. of South Hackensack, NJ) equipped with sigma mixing blades. The mixer was powered.by a ~ 60557-5540 3 Plasticorder, Model DR-2071, electronic torque rheometer with a Model FE-2000 interface (each of which are available from C. W. Brabender Instruments, Inc.).
The unvulcanized rubber ("Ameripol Synpol 8107") and rubbers ("Polysar S 1018" and "POLYSAR BUTYL XL
TM
68102").were added to the mixing chamber of the mixer and then blended for about 6 minutes at about 60 rpm.
The speed of the mixing blades was then reduced to 90 rpm, and the antioxidant (i.e., thiodiethylene bis-(3,5-di-tert-butyl-9-hydroxy) hydrocinnamate), 1s antiozonant (i.e., mixture o;f diaryl p-phenylene diamine), fumed silica, epoxy resin, iron oxide, boric oxide, melamine, and milled~glass fibers were added while mixing continued. The ingredients were mixed far about 3 minutes, after which the mixing speed was ' ZO increased to about 60 rpm. The plasticizer ("INDOPOL
H-100"') was then added, and mixing continued for about 13 minutes. The petrolatum was then slowly added and mixed in for about 5 minutes. Finally, the hydrated sodium silicate was added and mixed in for about 5 25 minutes. The batch sizes for Examples 1 and 2 were about 977 grams and about 462 grams, respectively.
The softness value of the putty was determined as-described above under the heading "Softness Value Measurement."' The softness value of both Examples 1 30 and 2 was 5.5 mm.
The char strength and expansion ratio (i~.e., the char volume divided by the initial volume) of each example was determined as follows. First, a portion of each putty was pressed to a thickness of about 0.635 cm 33 (1/4"). Next, a 2.5 cm (1 inch) diameter disc was die cut from each (pressed) sheet:.
The initial volume of each disc was determined by weighing the disc, coating the disc with wax by dipping R'O 96/20987 PCT/US95I16633 it in molten paraffin wax, submerging and weighing the (coated) disc in deionized water, and then calculating the volume using the following equation:
dry weight - submerged weight l0 volume =
- (Equation 1) density of water The disc was then placed in a muffle furnace at about 350°C for about 15 minutes to intumesce and char. The resulting charred, expanded disc was then weighed, coated with wax, and then submerged and weighed in deionized water. The volume of the charred, expanded disc was calculated using Equation 1 (above).
The expansion ratio was calculated using the following equation:
volume of charred, expanded disc volume =
(Equation 2 ) volume of initial (uncharred) disc The expansion ratios of Examples 1 and 2, based on an average of two determinations, were 2.84 and 5.22, respectively. The flow characteristics of the Example 1 and 2 putties were both excellent.
Examples 1 and 2 passed both the "Flame Through Test" and the "Fire Hose Stream Test."
Examples 3-10 The ingredients for Examples 3-10 are listed in Table 3, below.
o N o u~ 0 0 0 0 0 .-1 ~f1 Irl N N 1~1 Iff Uf ' a ~ ,.~
O O O O O O O O
a ~1 O Uf O O O O O
1p O 1~1 N . Ir! Uf N
p ~ ~
O O O O O O O O
' Uf O ff O O O O O
W ' ~i Nf N N Pf O If1 a ~ m .a .a r, .
y~ o 0 0 0 0 0 0 0 p ,..n o us o 0 0 0 0 1p O Nf N N PI .
f~ N .i .1 O O O O O O O O
.~/ r ~f1 O off O O O O O
~ N N ~
' N r1 O
f ~ 1 O Uf O O O O O
f n1 1p ~ O !~ N N Al vf1 off H O ~1 r1 .i ,~U1 O U1 O O O O O
, ~1 1'~1 N N ~'~f v1 ~I1 O
O O O O O O O O
Uf O off O O O O O
O O ~ N N wf h ~ ~ .a ~ N
o o .a 4 ~ ~. o a ~
v V y w N h ~ i~ i~ o~r >
i ~ , 11G w ~ w o t o ao v ' > r,. t~ w v~ a a~ ,o Z se tb > o ~n c ar o ar m b e.wa a H ~ w f.. o-m wer , w o v~r~rrir0 '00~ wZ aa~ ua C wpA
v H o ~w > w .1 o w ~. c: ~,y ..irr ..~
.w a.w ~
a .~ .~.o ac o s ~ a w .o ; s s w i m x s ~ - ~c c x ~ c m - o .~ yh .iws . wwo - a--N i ~
c0.
w o ~r o n o ~ w ~ o a f .a ~, ..r O a ~ w ucw a~.,o o ..i i w.-m..~ wca'= ..m ~
a ~
. aun o a~d~ wa~m ~n ~ b-..~o b >.o rood ~ a r~llo w vo tZ i G -.~
0 a i ' O
. . o w xCa: Z7oG...
a o, c b x a w i '~ o Ps S .a o o >.~o ~ v, o ~. o ..~ r~
a ,r b ,,, . ~ . . ~ , ..~
H i W = , f ,., N ~ _ t ~
.'i 0 V ~~'O H .ti w W 1 i1~ ri x L~ ~ ~ N 0 i '~' ~ O
A
i .a p O O 0 0 O O
. . . . .
O. O O O O O
h O O O O O O
a o 0 0 0 0 0 i o 0 o p ~ 0 o o ~
o e ~o .a .d " 0 o .,., " 0 0 0 0 0 0 o ~ ~n ~ n~ .~ ~o y V
~ 0 0 0 0 "~0 0 0 ' 0 0 0 0 0 0 1f~~ Nf 1~ 1p N
~i ,~0 0 0 0 0 0 Iff~ PI 1~ O N
O O O O O O
A O O O O O O
O O O ~ ~ O
r1 ~
Q i:
~ ~
~
11 I :
17 w~ i . ~
x O s a ~
o , ~ ~ o r ~p .r p .a .
.i ~ ~ .
a~a b 4yv~Gds a o '' a ~ g ~ ~
o ~W ov~ a~r~ r~.-aWa ~~Ca o a.a $o~ v a a ox sac a xw o~
.., o a ~
aw . . ..~
a ~ 4 ~ O d i~ A
. ~ 1 N W 'd .1 r1 a . ~
. ~ ~
~
H ! m iww ~ u w=~ t9.c . w Examples 3-10 were prepared as described for Examples 1 and 2. The batch size of each example was about 477 grams.
The expansion ratio of Examples 3-10 were , determined (as described in Examples 1 and 2) to be 3.06, 2.96, 3.05, 2.96, 3.02, 3.00, 3.07, and 3.10, respectfully. The softness values of the Example 3-10 putties were determined as described above under the heading "Softness Value Measurement." The softness values for Examples 3-10 were 5.6 mm, 5.7 mm, 5.6 mm, 5.8 mm, 6.0 mm, 5.8 mm, 5.9 mm, and 5.9 mm. The flow characteristic of the Examples 3-10 putties were excellent, excellent, excellent, excellent, very good, very good, good, and fair, respectively.
Examples 11-14 The ingredients for Examples 1l-14 are listed in Table 4, below.
Table 4 llmouat of ingredieata, Iags~edieat ?s.. ?~c. lac. l~c.
benzene sulfonyl hydrazide which decompose to give off gases. The amount of intumescent material in the formulation varies depending on the type of intumescent chosen.
The preferred intumescent material is a granular hydrated alkali metal silicate intumescent composition comprising a mixture of bound water; at least one alkali metal silicate having the formula MZO:xSi02 (e. g., sodium silicate, lithium silicate, and potassium silicate), wherein M is an alkali metal and x ranges from about 1.5 to about 4, and at least one oxy boron compound selected from the group consisting of boric acid and borate salts of group I and II elements (e. g., metaborate, tetraborate, perborate, polyborate radicals, boric acid, colemanite, calcium metaborate, magnesium borate, and zinc borate) (see, e.g., U.S.
Pat. No. 4,521,333 (Graham, et al.).
Preferably, the molar ratio of boron (present in the oxy boron compound) to M is between about 0.2 and about 0.9. The water preferably comprises about 5 to 15 percent by weight of the mixture of water, oxy boron compound(s), and alkali metal silicate(s).
Preferably, the intumescent material is added in particulate form to the rubber and unvulcanized rubber in an amount sufficient to allow the putty to pass the fire test described below under the heading "Flame Through Test," but not so much that it makes the putty non-pliable, or that it adversely affects the char that forms in a fire such that heated putty does not pass the Fire Hose Stream Test described below.
Typically, the amount o.E intumescent material (e. g. hydrated alkali metal silicate) used ranges from about 50 to about 200 percent (preferab:Ly about 100 to about 140 percent) by weight of the total vulcanized rubber and unvulcanized rubber content of thES putty. In another aspect, the hydrated alkali metal silicate preferable is present in the range from about 5 to about 45 percent by weight, based on the total weight of the putty.
The hydrated alkali metal silicate particles typically range in size from about 75 micrometers to about 500 micrometers.
A silicate intumescent material such as hydrated sodium silicate is preferably used together with a silicate fluxing agent such as boric oxide. Such fluxing agents are used to stabilize the char formed when the putty is subjected to heat. A preferred silicate fluxing agent is anhydrous boric oxide (B203) , commf~rcially available from U.S. Borax of Valencia, CA. Boric: oxide can function as both a flame retardant and a silicate fluxing agent.
If the intumescent material is intercalated graphite, the putty preferably comprises in the range from about 5 to about 30 percent by weight intumescent material, based on the total weight of the putty.
It is within the scope of the present invention to use combinations of intumescent material (e. g., to use both hydrated alkali metal silicate and intercalated graphite).
Preferably, a sufficient amount of plasticizer is included in the putty to obtain the desired level of softness and moldability. Plasticizers are compounds that increase the flexibility of a material and facilitate processing. Suitable plasticizers include 9a s aromatic oils, naphthenic oils, mineral oil, waxes, phthalate esters such as dioctyl phthalate (DOP) or dibutyl phthalate, and phosphate esters such as 2-ethylhexyl diphenyl phosphate (commercially available, for example, under the trade designation '"SANITIZER
141"' from Monsanto of St. Louis, MO), isodecyl diphenyl phosphate, or triaryl phosphate ester (commercially available, for example, under the trade designation TM
"SANITIZ~R 143"' from Monsanto). A preferred plasticizes is isobutylene/butene copolymer liquid 1s commercially available under the trade designation °INDOPOL H100" from Amoco Oil Co. of Chicago, IL.
Suitable waxes include petrolatum (commercially available, for example, under the trade designations' "6916 WA7CM~ and '"PAXWAX 5324~ from National Wax Division TM
of Dussek Campbell, Inc., Skokie, ~ IL: "'SR-172"' from .C.
TM
P. Hall Co. of Chicago, IL: and '"P~TROLATUM RP8"' from Witco Chemical Corp. of New York, NY).
Typically, the plasticizes is present in the range from about 30 to about 50 percent by weight (preferably, from about 35 to about 45 percent by weight, based on the total rubber and unvulcanized rubber content of the putty. In another aspect, the plasticizes typically is present, in the range from about 2 to about 25 percent by weight, based on the .
3o total weight of the putty.
Other optional ingredients that can be included in the putty formulation include flame retardants, char formers (e.g., char forming resins), fillers, colorants, antioxidants, and antiozonants.
3s Useful flame retardants include boric oxide: zinc borate: alumina trihydrate: nitrogen phosphates such as ethylene diamine phosphate (commercially available, for TM
example, under the trade designation '~AMGUARD ~DiAP"
~ 60557-5540 from Allright & Wilson Ltd. of Richmond, VA), dimelamine phosphate (commercially available, for example, under the trade designation ~AMGUARD ND"' from Allright & Wilson Ltd.), melamine phosphate (commercially available, for example, under the trade TM
to designation '"AMGUARD NH"' from Allright 6 Wilson Ltd. ) , ammonium polyphosphate (commercially available, for TM
example, under the trade designations "PHOS CHEK'P30"' TM
and "PROS CHEK P40~ from Monsan~o)~ and a blend of bis melaminium pentate and polyhedric oxide (commercially available, for example, under the trade designation TM
"CHAR GUARD 329" from Great Lakes Chemical Corp. of West Lafayette, IN).
Useful char forming resins include epoxy resins, phenolic resins, polycarboimide resins, urea-2o fonaaldehyde resins, and melamine-formaldehyde resins.
The general term "phenolic" refers to phenol-formaldehyde resins as well as resins comprising other phenol-derived compounds and formaldehydes. A
preferred char forming resin is an epoxy resin commercially available under the trade designation "SCOTCHCRST SR 265"' from the 3M Company of St. Paul, MN.
Fillers can used to adjust the hardness of the putty (i.e., fillers typically make the putty stiffer or harder), act as reinforcement, or reduce cost.
Fillers include fumed silica, clay, fly ash, colorants, perlite, venaiculite, inorganic fibers (e. g., glass fibers and mineral fibers), and organic fibers.
Melamine, which as discussed above is an organic intumescent material, is also useful as a filler to adjust the tack of the putty. A preferred filler is milled glass fiber (commercially available as "731ED
TM
FIBERGLAS" from Owens-Corning Fiberglas Corp. of ~ 60557-5540 S Toledo, OH), or chopped fiberglass fibers (commercially available, for example, under the trade designation ~799AB"' from Owens-Coming Fiberglas Corp. of Toledo, OH ) .
Colorants ( a . g . , iron oxide such as FeaO, or FeZ03 D
1o are useful for product' identification.
Antioxidants are compounds added to rubbers to protect the rubber against degradation by oxygen. Such compounds are typically comprised of aromatic amines.
Antiozonants may be used to protect the putty from 15 degradation by ozone. Some compounds may perform as antioxidants as well as antiozonants. A preferred antioxidant is thiodiethylene bis-(3,5-di-tert-butyl-9-hydroxy) hydrocinnamate (commercially available under r", .
the trade designation "IRGANOX 1035" from the Additives 2o Division of Ciba-Geigy Corp. of Hawthorne, NY).
A preferred antiozonant is a mixture of diaryl p-phenylene diamines (commercially available under the trade designation "WINGSTAY 100" from Goodyear Chemicals Division of Goodyear Tire and Rubber Co. of 25 Akron, OH) .
The putty can be made, by combining the ingredients used to make the putty using conventional techniques known in the art. Typically, the putty is made by mixing the various ingredients using a mogul mixer 3o equipped with circulating cooling water. The cooling water minimizes the build up of heat resulting from exothermic reaction of the ingredients and/or the action of mixing blades, therby preventing the intumescent material from prematurely intumescing.
3s Preferably, the rubber and unvulcanized rubber are added to the mixing chamber and mixed until thoroughly blended. Any fillers, silicate fluxing agents, char forming resins. waxes, colorants, flame retardant, lx melamine, antioxidants, and antiozonants are then added while the mixing operation continues. Plasticizer is typically added and then mixed in for a few minutes.
The last ingredient added is usually the intumescent material. The putty is typically mixed until l0 homogeneous and smooth (i.e., not lumpy). After mixing, the putty is ready to use.
For many firestop applications, the putty is typically extruded into sheets or pads (usually about 0.635 cm (0.25 inch thick). The sheets or pads are cut to provide the desired size or shape for a particular application. For some applications, the putty is formed into sticks or rope.
Objects and advantages of this invention are further illustrated by the following examples, but the particular materials and amounts thereof recited in these examples, as well as other conditions and details, should not be construed to unduly limit this invention. All parts and percentages are by weight unless otherwise indicated.
Softness Value Measurement The softness of the putty is determined using a penetrometer (available as Model 73510 from Precision Instruments of Chicago, IL). Measurement of the 3o softness of the putty involves dropping a weighted cone-shaped object into the putty, and then measuring the distance the object penetrates the putty. The test procedure is described in ASTM D-1403-91, which is entitled "Standard Test Methods for Cone Penetration of Lubricating Grease Using One-Quarter and One-Half Scale Cone Equipment," wherein the penetration measurements were made using a stainless steel, quarter scale cone as specified in the ASTM test method.
Specifically, the softness value of the putty was determined by packing the putty into a tube open at each end such that the putty was flush with both ends of the tube. The packed cylinder was allowed to stand , at room temperature (about 23°C) for a minimum of 12 to hours before the softness value was determined. -The cone and the shaft connected thereto weighed 9.38_+0.025 grams. An additional 150 grams was added to the top of the shaft. The tip of the cone-shaped object was placed so it just touched the surface of the putty packed into cylinder. For each measurement, the shaft was released and the cone allowed to sink into the putty for 5 seconds. The distance the cone sank into the putty during the 5 seconds was recorded. The softness values reported for Examples 1, 2, and 20 are 2o based on an average of 2 measurements. The softness values reported for Examples 3-19 are based on an average of 10 measurements.
Putty Flow Measurement Putty was packed into a tube (2.5 cm diameters 2.5 cm long) open at each end such that it was flush with both ends of the tube. The packed tube was then laid on its curved side in an oven at 200°C for 30 minutes.
The amount of flow that occurred during the 30 minutes of heating was determined visually to be excellent (i.e., no flow), very good (i.e., slight flow), good (i.e., some flow, but material did not flow onto the surface on which the tube was placed in the oven), fair, or very bad (i.e., material flowed freely out of the tube and onto the surface on which the tube was placed in the oven).
Flame Through Test The Flame Through Test follows the procedure set forth in ASTM'(American Society for Testing Materials) Test '"E 819-83,"' entitled "Standard Test Method for Fire Tests of Through-Penetration Fire Stops".
to This test is used to evaluate the use of putty in a through-penetration tire application.
For this test, a poured concrete slab, 11.4 cm .(4.5 in) thick and approximately 30.5 cm (3 ft) square, was prepared. Four 10.2 cm (9 in) diameter circular openings were made in the slab. The openings were evenly spaced. A 2.5 cm (1 in)) thick mineral fiber insulation material (commercially available under the trade designation. "USG 114 FIRE SAFING" from US .
2o Gypsum of Chicago, IL) was firmly packed into each .
opening in the slab. The mineral fiber was recessed about 2.5 cm from the top surface of the concrete. The putty was packed into the opening flush with the top surface of the concrete. The thickness 'of the putty was about 2.5 cm. The concrete slab was placed on the top of a gas-fired furnace (commercially available from Armil C.F.S. of South Iiolland, IL). The mineral fibers faced the heat source (flame) of the furnace.
The time and temperature parameters outlined in Figure 1 of ASTM E 819-B3 were followed for the test.
The test was run for 3 hours. unless flame through occurred. Flame through is indicated by flames coming through the opening to the "cold" side of the concrete slab. If there is flame through in less than 3 hours, then the material tested is deemed to have failed the test. If the opening remained sealed for the.3 hours, then the fire stop is given a passing designation (referred in ASTM E 819-83 as having an "F" rating).
Fire Hose Stream Test If a fire stop employing the putty of one of the examples passed the "Flame Through Test," then the following test, which is described in ASTM E 814-83, l0 was conducted.
Immediately after the "Flame Through Test," the slab was removed from the furnace and placed vertically in a metal stand. From a distance of 6.1 meters (20 ft), a stream of water was propelled in a sweeping motion against the material in the opening of the concrete slab at a pressure of 0.21 MPa (30 lbs/in2 ).
To pass this test, the material sealing the through-penetration, after having been subjected to the heat from a fire thus producing a char, had to withstand the 2o hose stream and continue to seal the pipe for a period of 1.5 seconds per 0.09 square meter,(i.e., 1.5 seconds per square foot) of test structure. For example, a 0.84 m2 (9 ft2) assembly must withstand a hose stream for 13.5 seconds.
~ 60557-5540 The ingredients used for the examples are listed in Table 1, below.
Table 1 Iags~edibat Trades Desigiution loaroa of Ingradieat Uavulcaaised styrene'"AMERIP01. SYNPOb Ameripol Syapol butadiene rubber 8107'x" Co. Division bf Uairoyal Goodrich Tire ' Co., Akso~n, OH
Styrene butadiene '"POLYSAR S lOlB"''"~Polysar Rubber rubber ~ Division of ' Milan, Pittsburgh, PA
Moderately "POLYSAR BUTYL Xh Polysar Rubber ~
crosslinked butyl 68102'T~ Division of rubbez Idiles, Pittaburgh, PA
Mixture of diaryl '"wINGSTAY 100'T~ Goodyear .
p-pheaylene diamine Chemicals Division of Goodyear Tise and R~bbes Co,., Jv)cron, Thiodiethyleae bin-"IRGANOX 1035' .W dditivea (3,5-di-tert-butyl-~- Division of hydroxy) Ciba-Geigy hydrocianaaate Corp., Narrthorne, NY
Fumed silica "CAB-O-SIL M-5" ~ Cabot Corp., .
Tuscola, II.
Epoxy resin po~rder'"SCOTCHCAST SR-265'The 3M Company, St. Paul, 1~1 Pos~dered iron oxide"IRON OXIDE BF-95"' Bailey (Fe=0>> Fagineers, Iae., Fairfield, AL
Soroa trioxide powder"ANHYDROUS BORIC tl.S. Borax, ACID"' ~" Valencia, G
Melamine po~dtr "AFRO MEIJ~MINE" Cytec (-60 ~
mesh) Industries, west Peterson, NJ
Milled glass '"?3~ED FIBERGLASS Oweas-Corafag, filaments 1/e""""~ Fiberglas Corp., Toledo, OH
Table 1 Continued Milled glaaa . "MFX-ll- 8 IN Phoenix filaments Fiberglas, Inc., oakville, Ontario, Canadi Chopped fiberglass "799A8"'r' . Ovens-Corning ' fibers, 1.25.cm Fiberglas Corp., (0.5 inch) lon Toledo, OH
Isobutylene butane '"INDOPOL H-~100"'~Amoco Chemical c of r 1i d Co., Chica , Ib Copolyaer of isobutyl'"POLYSAR BUTYL. Polysar Rubber 301"' and isoprene Division of Miles Petrolatum '"6916 i~A7C"~" Nation: Wax .
Division of Dussek Campbell, Ine., Skokie, IL
Petrolatum '"PA)CWAX 532"'"" Natioat Wax Division of Dussek Campbell.
Inc.
Petrolatum "PEN~~ ~~"' ~" Peareco zproducts C.;
Peateco Division, ICarns Cit , PA
Petrolatum '"PETROLATUM RP$'"7"'Witco Chemical Corp., Nsw York, NY
Blend of bis "CHARGUARD 32g'"" Grsat Lakes melaminium pentate Chemical Corp., and polyhedric oxide West Lafayette, (flame retardant) Intercalated graphite"GRAPHITE TG 326"'x"UGR Carbon Co., , flake ~ Inc., Danbury, Granulated hydrated'"EXPANTROL ~811"'~The 3M Company sodium silicate Granulated hydrated"EXPANTROL 2"''". The 3M Company sodium silicate Hydrated zinc borate"FIREBRAKE Z8 FINE""U.S. Horax i n. 1 II~.n~ I
a 60557-5540 Examples 1 and 2 The ingredients for Examples 1 and 2 are listed in Table 2, below.
Table 2 llmonn! of Ingredients, pgit~
Zagrediea! Example 1 P~cample Unvulcanized atysene 76.50 76.50 butadiene rubber ("AI~RIPOI. SYNPOI.
B107"')1""
Styrene butadiene rubber 20.00 20.00 ("POhYSAR S 1018")1""
Moderately croaslinked yl 3.50 3.50 but rubber ('POLYSAR XI. ~"
68102"'~
Mixture of diaryl p-phenylene 2.00 2.00 diamine ("NINGSTAY 100")s Thiodiethylene bin-(3,5-di-tert- 2.00 2.00 butyl-4-hydroxy) hydrocinnamate ('"IRG~1NOX 1035")1'"
Fumed silica ('"CA8-O-SII. 13.00 13:00 M 5"'JTM
Epoxy resin powder ("SCOTCHCAST 15.00 15.00 8R 265")1""
Powdered iron oxide 5.00 5.00 (FeZO~) ("IRON OXIDE BF 95"')TM
Melamine powder ('"HERO 50.00 75.00 , MELAMINE"' ) r"' Boron Oxide 10.00 X0.00 (Anh roua) Milled glass filaments 30.00 30.00 ('"731ED
FI BERGIJ4SS" f"
Isobutylene butane copolysier X0.00 50.00 1i id ("INDOPOh H 100")TM
Petrolatum ('"6916 WAX"')' 60.00 60.00 Granulated hydrated.spdium 120.00 silicate ('"EXPANTROI.
481"')1'"
Intercalated graphite ?0.00 flake ("GRAPHITE TG 326"')r'"
* Parts per hundred based on the total rubber sad unvulcanized rubber content of the putty.
The ingredients for each example were compounded ,15 using an internal mixer (Prep Mixer, Part # 02-2~-000, 350/420 cm' capacity: available from C. W. Hrabender Instruments, Inc. of South Hackensack, NJ) equipped with sigma mixing blades. The mixer was powered.by a ~ 60557-5540 3 Plasticorder, Model DR-2071, electronic torque rheometer with a Model FE-2000 interface (each of which are available from C. W. Brabender Instruments, Inc.).
The unvulcanized rubber ("Ameripol Synpol 8107") and rubbers ("Polysar S 1018" and "POLYSAR BUTYL XL
TM
68102").were added to the mixing chamber of the mixer and then blended for about 6 minutes at about 60 rpm.
The speed of the mixing blades was then reduced to 90 rpm, and the antioxidant (i.e., thiodiethylene bis-(3,5-di-tert-butyl-9-hydroxy) hydrocinnamate), 1s antiozonant (i.e., mixture o;f diaryl p-phenylene diamine), fumed silica, epoxy resin, iron oxide, boric oxide, melamine, and milled~glass fibers were added while mixing continued. The ingredients were mixed far about 3 minutes, after which the mixing speed was ' ZO increased to about 60 rpm. The plasticizer ("INDOPOL
H-100"') was then added, and mixing continued for about 13 minutes. The petrolatum was then slowly added and mixed in for about 5 minutes. Finally, the hydrated sodium silicate was added and mixed in for about 5 25 minutes. The batch sizes for Examples 1 and 2 were about 977 grams and about 462 grams, respectively.
The softness value of the putty was determined as-described above under the heading "Softness Value Measurement."' The softness value of both Examples 1 30 and 2 was 5.5 mm.
The char strength and expansion ratio (i~.e., the char volume divided by the initial volume) of each example was determined as follows. First, a portion of each putty was pressed to a thickness of about 0.635 cm 33 (1/4"). Next, a 2.5 cm (1 inch) diameter disc was die cut from each (pressed) sheet:.
The initial volume of each disc was determined by weighing the disc, coating the disc with wax by dipping R'O 96/20987 PCT/US95I16633 it in molten paraffin wax, submerging and weighing the (coated) disc in deionized water, and then calculating the volume using the following equation:
dry weight - submerged weight l0 volume =
- (Equation 1) density of water The disc was then placed in a muffle furnace at about 350°C for about 15 minutes to intumesce and char. The resulting charred, expanded disc was then weighed, coated with wax, and then submerged and weighed in deionized water. The volume of the charred, expanded disc was calculated using Equation 1 (above).
The expansion ratio was calculated using the following equation:
volume of charred, expanded disc volume =
(Equation 2 ) volume of initial (uncharred) disc The expansion ratios of Examples 1 and 2, based on an average of two determinations, were 2.84 and 5.22, respectively. The flow characteristics of the Example 1 and 2 putties were both excellent.
Examples 1 and 2 passed both the "Flame Through Test" and the "Fire Hose Stream Test."
Examples 3-10 The ingredients for Examples 3-10 are listed in Table 3, below.
o N o u~ 0 0 0 0 0 .-1 ~f1 Irl N N 1~1 Iff Uf ' a ~ ,.~
O O O O O O O O
a ~1 O Uf O O O O O
1p O 1~1 N . Ir! Uf N
p ~ ~
O O O O O O O O
' Uf O ff O O O O O
W ' ~i Nf N N Pf O If1 a ~ m .a .a r, .
y~ o 0 0 0 0 0 0 0 p ,..n o us o 0 0 0 0 1p O Nf N N PI .
f~ N .i .1 O O O O O O O O
.~/ r ~f1 O off O O O O O
~ N N ~
' N r1 O
f ~ 1 O Uf O O O O O
f n1 1p ~ O !~ N N Al vf1 off H O ~1 r1 .i ,~U1 O U1 O O O O O
, ~1 1'~1 N N ~'~f v1 ~I1 O
O O O O O O O O
Uf O off O O O O O
O O ~ N N wf h ~ ~ .a ~ N
o o .a 4 ~ ~. o a ~
v V y w N h ~ i~ i~ o~r >
i ~ , 11G w ~ w o t o ao v ' > r,. t~ w v~ a a~ ,o Z se tb > o ~n c ar o ar m b e.wa a H ~ w f.. o-m wer , w o v~r~rrir0 '00~ wZ aa~ ua C wpA
v H o ~w > w .1 o w ~. c: ~,y ..irr ..~
.w a.w ~
a .~ .~.o ac o s ~ a w .o ; s s w i m x s ~ - ~c c x ~ c m - o .~ yh .iws . wwo - a--N i ~
c0.
w o ~r o n o ~ w ~ o a f .a ~, ..r O a ~ w ucw a~.,o o ..i i w.-m..~ wca'= ..m ~
a ~
. aun o a~d~ wa~m ~n ~ b-..~o b >.o rood ~ a r~llo w vo tZ i G -.~
0 a i ' O
. . o w xCa: Z7oG...
a o, c b x a w i '~ o Ps S .a o o >.~o ~ v, o ~. o ..~ r~
a ,r b ,,, . ~ . . ~ , ..~
H i W = , f ,., N ~ _ t ~
.'i 0 V ~~'O H .ti w W 1 i1~ ri x L~ ~ ~ N 0 i '~' ~ O
A
i .a p O O 0 0 O O
. . . . .
O. O O O O O
h O O O O O O
a o 0 0 0 0 0 i o 0 o p ~ 0 o o ~
o e ~o .a .d " 0 o .,., " 0 0 0 0 0 0 o ~ ~n ~ n~ .~ ~o y V
~ 0 0 0 0 "~0 0 0 ' 0 0 0 0 0 0 1f~~ Nf 1~ 1p N
~i ,~0 0 0 0 0 0 Iff~ PI 1~ O N
O O O O O O
A O O O O O O
O O O ~ ~ O
r1 ~
Q i:
~ ~
~
11 I :
17 w~ i . ~
x O s a ~
o , ~ ~ o r ~p .r p .a .
.i ~ ~ .
a~a b 4yv~Gds a o '' a ~ g ~ ~
o ~W ov~ a~r~ r~.-aWa ~~Ca o a.a $o~ v a a ox sac a xw o~
.., o a ~
aw . . ..~
a ~ 4 ~ O d i~ A
. ~ 1 N W 'd .1 r1 a . ~
. ~ ~
~
H ! m iww ~ u w=~ t9.c . w Examples 3-10 were prepared as described for Examples 1 and 2. The batch size of each example was about 477 grams.
The expansion ratio of Examples 3-10 were , determined (as described in Examples 1 and 2) to be 3.06, 2.96, 3.05, 2.96, 3.02, 3.00, 3.07, and 3.10, respectfully. The softness values of the Example 3-10 putties were determined as described above under the heading "Softness Value Measurement." The softness values for Examples 3-10 were 5.6 mm, 5.7 mm, 5.6 mm, 5.8 mm, 6.0 mm, 5.8 mm, 5.9 mm, and 5.9 mm. The flow characteristic of the Examples 3-10 putties were excellent, excellent, excellent, excellent, very good, very good, good, and fair, respectively.
Examples 11-14 The ingredients for Examples 1l-14 are listed in Table 4, below.
Table 4 llmouat of ingredieata, Iags~edieat ?s.. ?~c. lac. l~c.
Unwlcanized styrene butadiene76.50 76.50 76.50 76.50 ( "AMERI POL SYNPOL 8107 "' ) r""
Styrene butadiene rubber 20:00 20.00 20.00 20.00 ("POLYSAR ~S 1018' )'"' Moderately crosalinked butyl3.50 3.50 3.50 3.50 rubber (POLYSAR XL 68102"')1""
Mixture of diaryl p-phenylene2.00 2.00 2.00 2.00 diamine ('"WINGSTAY 100"')T~
Thiodiethylene bia-(3,5-di-2.00 2.00 2.00 2.00 tart-butyl-4-hydroxy) hydrocinnamate ("IRGANOX
1035")TM
Fumed silica ('CAB-O-SIL 13.00 13.00 13.00 13.00 M 5"')TM.
Epoxy resin powder 7.5.00 15.00 15.00 15.00 ("SCOTCHCAST SR 265"')TM
Powdered iron oxide (FezO~)5.00 5.00 5.00 5.00 ("IRON OXIDE BF 95"') T""
Melamine powder ("HERO 50.00 50.00 50.00 50.00 MELAMINE" ) T""
Boron Oxide 90.00 (anh roua) Hydrated Zinc Borate 40.00 83.25 ("FIREBRAKE ZB FINE"')1M
Milled glass filaments ('"731ED30.00 30.00 30.00 30.00 FI BERGIJ~SS "' ) T""
Isobutylene butane copolymer,40.00 40.00 40.00 40.00 1i id ('"INDOPOL H 100"')1""
Petrolatum ("PAXWAX 5324"')T~~60.00 60.00 60.00 60.00 Granulated hydrated sodium 120.00 120.00 120.00 120.0 silicate ('"EXPANTROL 4BW"')TM 0 to Examples 11-14 were prepared by blending the styrene butadiene rubbers ("POLYSAR S 1018"r""and "POLYSAR XL 68102")1; and about 4.35% of the unvulcanized styrene butadiene rubber ("AMERIPOL SYNPOL
8107")TM on a 40.6 cm (16 inch) rubber mill, and then mixing for about 30 minutes at about 20 rpm. About 3.75% of the plasticizer ("INDOPOL H-100")'Mesas then added to the rubber/unvulcanized rubber mixture while milling continued.
~ 60557-5540 The resulting "prebatch" was removed from the rubber mill and charged into a mogul mixer (No. 59821:
available from APV Chemical Machinery Inc. of Saginaw, MI) along with the balance of the unvulcanized styrene butadiene rubber("AMERIPOL SYNPOL 8107")T;and then mixed 1o for about 2 minutes.
While mixing continued, antioxidant (i.e., , thiodiethylene bis-(3,5-di-test-butyl-4-hydroxy) hydrocinnamate), antiozonant (i.e., the mixture of diaryl p-phenylene diamine), fumed silica, epoxy resin, 13 iron oxide, boron oxide (if in the formulation), zinc borate (if in the formulation), melamine, and milled glass fibers were added to the mixer over a 10 minute period. Plasticizes ("INDOPO:L H-100"Tj was then added and mixed in for about 5 minutes. Next, hydrated 20 sodium silicate ("EXPANTROL 48W") was added and mixed in for about S~minutes. Finally, the petrolatum ("PAXWAX 5324"'jMwas added and mixed in for about 10 minutes, until the putty was smooth. The batch sizes ' of Examples 11-14 were about :L.35 kg, about 1.35 kg, 25 about 1.24 kg, and about 1.47 kg, respectively.
The expansion ratio of Examples 11-l4 were determined (as described in Examples 1 and 2) to be 2.77, 2.77, 3.20, and 2.64, respectively. The softness values of the Example 11-14 putties were determined as 3o described above under the heading "Softness Value Measurement." The softness values for Examples 11-14 were 5.4 mm, 5.5 mm, 5.5 mm, and 5.10 mm, respectfully.
The flow characteristic of the Examples 11-14 putties were excellent, good, good, and very good.
33 The "Flame Through Test" and the "Hose Stream Test" were run on four samples of each lot. All four samples for Examples 11, 13, and 14 passed the "Flame Through Test." Only two of the four Example 12 i i . I I I"~ I
~ 60557-5540 samples, however, passed the "Flame Through Test."' For the "Hose Stream Test," four of the Example 11 samples passed, one of the Example 12 samples passed, none of the Example 13 samples passed,. and three of the Example 14 samples passed.
1o Examples. 15-19 The ingredients for Examples 15-19 are listed in Table 5, below.
TABLE 5 .
lvmonat f ingredients o , Pit Ingredient l~c. l~c. lac. ~c. 18 ?ac.
Unvulcanized 76.50 76.50 76.50 76.50 76.50 styrene , butadiene rubber '"AMERI POI.
SYNPOI. 8107"' )T""
Styrene 20.00 20.00 20.00 20.00 20:00 butadiene rubber ('" POLYSAR
S
lore-jTM
Moderately 3.50 3.50 3.50 3.50 3.50 croaslinked butyl rubber ('"POLYS1\R
XI.
68102"'jT""
Mixture of 2.00 2.00 2.00 2.00 2.00 diaryl p-phenylene diamine (WINGSTAY 100')TM
Thiodiethylene 2.00 2.00 2.00 2.00 2.00 bis-(3,5-di-tert-butyl-4-hydroxy) hydrocinnamate ("IRGANOX 1035"')""
Fumed silica 13.00 13.00 13.00 13.00 13.00 ('" CAB-O-S
I I. M
5.j,~
Epoxy resin 15.00 15.00 15.00 15.00 15.00 powder ('"SCOTCHCAST
SR
265"')T""
Powdered iron 5.00 5.00 5.00 5.00 5.00 oxide (FeiO~) ("IRON OXIDE
BF
95"')rra ~ 60557-5540 Table 5 Continued I~lelamine powder50.00 50.00 50.00 50.00 50.00 ("~
Z'~L~MII~iL""
)'"
Boson oxide 10.00 40.00 10.00 10.00 10.00 lanh rows) Killed glass -30.00 filamenta 30.00 30.00 30.00 30.00 ("731LrD
FTBERGI~'1SS"
) "'' Iso~tyle~ 55.00 50.00 10.00 0.0 25.00 buteae ex~poiys~er liquid ("hIDOPO3.
H 100"') T~"
Petroiat~m 60.00 60.00 60.00 60.00 60.00 ("PAX~PA)C 532!")T"
Granulated 120.00 120.00 120.00 120.00 120.00 hydrated~sodium silicate "EXPI~iTWOI~
4 B11" )" .
Examples 15-19 were prepared as described for Examples l and 2. The batch size for Examples 15, 1-6, 17, 18, and 19, was about 992 grams, about 48? grams, about 977 grams, about 467 grams, and about 462 grams, to respectively.
The expansion ratio of Examples 15, 16, 17, 18, and 19 were determined (as described in Examples 1 and 2) to be 2.97, 2.93, 3.02, 2.97, and 2.93, respectively. The softness~values of the Example 3-10 putties were determined as described above under the heading '"Softness Value Measurement."' The softness values for Examples 15, 16, 17, 18, and 19 were 6.1 mm, 5.9 mm, 6.0 mm, 5.9 mm, and 5.1. mm, respectfully. The flow characteristic of the Examples 15, 16, 17, 18, and 19 putties were fairy good, very good, very good, and very good, respectively.
The following observations were made when handling each of Examples 15-19. Example 15 was very tacky and left residue on the skin. Example 16 was tacky and Z5 left some residue on the skin. Examples 17, 18, and 19 ~ 60557-5540 all had a good level of tackiness and left no visible residue on the skin.
Example 20 The ingredients for Example 20 are listed in Table 6, below.
Table 6 7lmonat o! ingredients, Ingredfeat gamble 20 Non-crosslinked 80.00 styrene butadiene rubber ('"AMERIPOL
SYNPOL
8107"')""' Cross-linked 20.00 styrene butadiene rubber ('"POLYSI\R
S
1018") T''"
Fumed 13.00 silica ("CAB-O-SIL
M-5"')T""
Epoxy 15.00 resin powder ("SCOTCIiCAST
SR
265"' ) T""' Powdered 5.00 iron oxide (FeZO~) ("IRON
OXIDE
BF
95')T""
Hydrated 50.00 zinc borate ("FIREBRAKE
ZB
FINE"')T"' Choed fiber lass fibers 20.00 ("799AB"')T""
Isobutylene 71.00 butene copolymer liquid ("INDOPOL
H
100"' ) TM
Blend 15.00 of bis melaminium pentate and of hedric oxide ('"C~iARGUARD
329"')x"
Petrolatum TM 50.00 ('"PETROLATUM
RPB"'T
Granulated 100.00 hydrated sodium silicate ('"EXPANTROL
2")'"' Example 20 was prepared as described for Examples 1 and 2. The batch size was about 439 grams.
The expansion ratio of Example -20 was determined (as described in Examples 1 and 2) to be 7.05. The softness value was determined as described above under the heading "Softness Value Measurement" to be 5.6 mm.
The flow characteristic of the putty was good.
Example 20 passed both the "Flame Through Test"
and the "Fire Hose Stream Test.."
Example 21 The ingredients for Example 21 are listed in Table ~7, below.
Table 7 Amount of ' Ingredieats PHR*
Ingredient Example 21 tlnvulcaaised styrene 74.02 butadiene rubber ("AMERIPOL SYNPOL 8109"ITM
Styzene butadiene rubber 22.11 ("Polysar S
1018") ""
Moderately crosslinked 3.8?
butyl rubber ( POLYSAR XL 68102")'"' Thiodiethylene bas-(3,5-di-tart- 3.32 butyl-4-hydroxy) hydrocinnamate ("IRGANOX 1035")T""
Flamed silica ("CAB-O-SIL"!~" 14.3?
E ox resin owder ("SCOTCHCAST 16.59 265" T""
Powdered iron oxide ( 5. 53 F'e203 ) ( "IRON
OXIDE BF-1")'~"
Melamine oWder ("HERO 55.29 MELAMINE")T""
Boron Oxide Anhydrous 44.23 ("BORIC OXIDE
60 MESH)T""
Milled filaments ("MFX-1/8'TM 33.1?
IN") Iaobutylene butane copolymer 44.23 liqisid ( "INDOPOL H 100" )T""
Petrolatum ("PENRECO AMBER")TM- 66.34 Granulated hydrated sodium 132.68 silicate "EXPANTROL 4B~" ) r''"
Parts pu hundred based on the fatal robber and unvulcaaized rubber cf the pnay. ' The ingredients were compounded using the internal mixer described in Example 1.
The unwlcanized rubber ("Ameripol Synpol 810?N),M
and rubbers ("Polysar S 1018" and "POLYSAR BUTYL XL
68102~') were added to the mixing chamber of the mixer and then blended for about 6 minutes at about 60 rpm.
2o The speed of the mixing blades was then reduced to 90 rpm, and the antioxidant (i.e., thiodiethylene bis-(3,5-di-tart-butyl-4-hydroxy) hydrocinnamate), fumed silica, epoxy resin, iron oxide, boric oxide, melamine, s and milled glass fibers were added while mixing continued. The ingredients were mixed for about 3 minutes, after which the mixing speed was increased to . about 60 rpm. The plasticizes ("INDOPOL H-100")'was then added, and mixing continued for about 13 minutes.
The petrolatum was then slowly added and mixed in for about 5 minutes. Finally, the hydrated sodium silicate was added and mixed in for about 5 minutes. The bhtch size was about 466.44 grams.
The softness value of the putty, as determined is using the method described above under the heading "Softness Value Measurement"',was 6.32 mm. The expansion ratio of Example 21,, based on an average of two determinations, was 2.76. The flow characteristic of the putty. was excellent. ,'E~rther, the '"Flame 2o Through Test"' and the '"Fire Hose Stream Test."' Various modifications and alterations of this invention will become apparent to those skilled in the art without departing from the scope and spirit of this 25 invention. and it should be understood that this invention is not to be unduly limited to the illustrative embodiments set forth herein.
Styrene butadiene rubber 20:00 20.00 20.00 20.00 ("POLYSAR ~S 1018' )'"' Moderately crosalinked butyl3.50 3.50 3.50 3.50 rubber (POLYSAR XL 68102"')1""
Mixture of diaryl p-phenylene2.00 2.00 2.00 2.00 diamine ('"WINGSTAY 100"')T~
Thiodiethylene bia-(3,5-di-2.00 2.00 2.00 2.00 tart-butyl-4-hydroxy) hydrocinnamate ("IRGANOX
1035")TM
Fumed silica ('CAB-O-SIL 13.00 13.00 13.00 13.00 M 5"')TM.
Epoxy resin powder 7.5.00 15.00 15.00 15.00 ("SCOTCHCAST SR 265"')TM
Powdered iron oxide (FezO~)5.00 5.00 5.00 5.00 ("IRON OXIDE BF 95"') T""
Melamine powder ("HERO 50.00 50.00 50.00 50.00 MELAMINE" ) T""
Boron Oxide 90.00 (anh roua) Hydrated Zinc Borate 40.00 83.25 ("FIREBRAKE ZB FINE"')1M
Milled glass filaments ('"731ED30.00 30.00 30.00 30.00 FI BERGIJ~SS "' ) T""
Isobutylene butane copolymer,40.00 40.00 40.00 40.00 1i id ('"INDOPOL H 100"')1""
Petrolatum ("PAXWAX 5324"')T~~60.00 60.00 60.00 60.00 Granulated hydrated sodium 120.00 120.00 120.00 120.0 silicate ('"EXPANTROL 4BW"')TM 0 to Examples 11-14 were prepared by blending the styrene butadiene rubbers ("POLYSAR S 1018"r""and "POLYSAR XL 68102")1; and about 4.35% of the unvulcanized styrene butadiene rubber ("AMERIPOL SYNPOL
8107")TM on a 40.6 cm (16 inch) rubber mill, and then mixing for about 30 minutes at about 20 rpm. About 3.75% of the plasticizer ("INDOPOL H-100")'Mesas then added to the rubber/unvulcanized rubber mixture while milling continued.
~ 60557-5540 The resulting "prebatch" was removed from the rubber mill and charged into a mogul mixer (No. 59821:
available from APV Chemical Machinery Inc. of Saginaw, MI) along with the balance of the unvulcanized styrene butadiene rubber("AMERIPOL SYNPOL 8107")T;and then mixed 1o for about 2 minutes.
While mixing continued, antioxidant (i.e., , thiodiethylene bis-(3,5-di-test-butyl-4-hydroxy) hydrocinnamate), antiozonant (i.e., the mixture of diaryl p-phenylene diamine), fumed silica, epoxy resin, 13 iron oxide, boron oxide (if in the formulation), zinc borate (if in the formulation), melamine, and milled glass fibers were added to the mixer over a 10 minute period. Plasticizes ("INDOPO:L H-100"Tj was then added and mixed in for about 5 minutes. Next, hydrated 20 sodium silicate ("EXPANTROL 48W") was added and mixed in for about S~minutes. Finally, the petrolatum ("PAXWAX 5324"'jMwas added and mixed in for about 10 minutes, until the putty was smooth. The batch sizes ' of Examples 11-14 were about :L.35 kg, about 1.35 kg, 25 about 1.24 kg, and about 1.47 kg, respectively.
The expansion ratio of Examples 11-l4 were determined (as described in Examples 1 and 2) to be 2.77, 2.77, 3.20, and 2.64, respectively. The softness values of the Example 11-14 putties were determined as 3o described above under the heading "Softness Value Measurement." The softness values for Examples 11-14 were 5.4 mm, 5.5 mm, 5.5 mm, and 5.10 mm, respectfully.
The flow characteristic of the Examples 11-14 putties were excellent, good, good, and very good.
33 The "Flame Through Test" and the "Hose Stream Test" were run on four samples of each lot. All four samples for Examples 11, 13, and 14 passed the "Flame Through Test." Only two of the four Example 12 i i . I I I"~ I
~ 60557-5540 samples, however, passed the "Flame Through Test."' For the "Hose Stream Test," four of the Example 11 samples passed, one of the Example 12 samples passed, none of the Example 13 samples passed,. and three of the Example 14 samples passed.
1o Examples. 15-19 The ingredients for Examples 15-19 are listed in Table 5, below.
TABLE 5 .
lvmonat f ingredients o , Pit Ingredient l~c. l~c. lac. ~c. 18 ?ac.
Unvulcanized 76.50 76.50 76.50 76.50 76.50 styrene , butadiene rubber '"AMERI POI.
SYNPOI. 8107"' )T""
Styrene 20.00 20.00 20.00 20.00 20:00 butadiene rubber ('" POLYSAR
S
lore-jTM
Moderately 3.50 3.50 3.50 3.50 3.50 croaslinked butyl rubber ('"POLYS1\R
XI.
68102"'jT""
Mixture of 2.00 2.00 2.00 2.00 2.00 diaryl p-phenylene diamine (WINGSTAY 100')TM
Thiodiethylene 2.00 2.00 2.00 2.00 2.00 bis-(3,5-di-tert-butyl-4-hydroxy) hydrocinnamate ("IRGANOX 1035"')""
Fumed silica 13.00 13.00 13.00 13.00 13.00 ('" CAB-O-S
I I. M
5.j,~
Epoxy resin 15.00 15.00 15.00 15.00 15.00 powder ('"SCOTCHCAST
SR
265"')T""
Powdered iron 5.00 5.00 5.00 5.00 5.00 oxide (FeiO~) ("IRON OXIDE
BF
95"')rra ~ 60557-5540 Table 5 Continued I~lelamine powder50.00 50.00 50.00 50.00 50.00 ("~
Z'~L~MII~iL""
)'"
Boson oxide 10.00 40.00 10.00 10.00 10.00 lanh rows) Killed glass -30.00 filamenta 30.00 30.00 30.00 30.00 ("731LrD
FTBERGI~'1SS"
) "'' Iso~tyle~ 55.00 50.00 10.00 0.0 25.00 buteae ex~poiys~er liquid ("hIDOPO3.
H 100"') T~"
Petroiat~m 60.00 60.00 60.00 60.00 60.00 ("PAX~PA)C 532!")T"
Granulated 120.00 120.00 120.00 120.00 120.00 hydrated~sodium silicate "EXPI~iTWOI~
4 B11" )" .
Examples 15-19 were prepared as described for Examples l and 2. The batch size for Examples 15, 1-6, 17, 18, and 19, was about 992 grams, about 48? grams, about 977 grams, about 467 grams, and about 462 grams, to respectively.
The expansion ratio of Examples 15, 16, 17, 18, and 19 were determined (as described in Examples 1 and 2) to be 2.97, 2.93, 3.02, 2.97, and 2.93, respectively. The softness~values of the Example 3-10 putties were determined as described above under the heading '"Softness Value Measurement."' The softness values for Examples 15, 16, 17, 18, and 19 were 6.1 mm, 5.9 mm, 6.0 mm, 5.9 mm, and 5.1. mm, respectfully. The flow characteristic of the Examples 15, 16, 17, 18, and 19 putties were fairy good, very good, very good, and very good, respectively.
The following observations were made when handling each of Examples 15-19. Example 15 was very tacky and left residue on the skin. Example 16 was tacky and Z5 left some residue on the skin. Examples 17, 18, and 19 ~ 60557-5540 all had a good level of tackiness and left no visible residue on the skin.
Example 20 The ingredients for Example 20 are listed in Table 6, below.
Table 6 7lmonat o! ingredients, Ingredfeat gamble 20 Non-crosslinked 80.00 styrene butadiene rubber ('"AMERIPOL
SYNPOL
8107"')""' Cross-linked 20.00 styrene butadiene rubber ('"POLYSI\R
S
1018") T''"
Fumed 13.00 silica ("CAB-O-SIL
M-5"')T""
Epoxy 15.00 resin powder ("SCOTCIiCAST
SR
265"' ) T""' Powdered 5.00 iron oxide (FeZO~) ("IRON
OXIDE
BF
95')T""
Hydrated 50.00 zinc borate ("FIREBRAKE
ZB
FINE"')T"' Choed fiber lass fibers 20.00 ("799AB"')T""
Isobutylene 71.00 butene copolymer liquid ("INDOPOL
H
100"' ) TM
Blend 15.00 of bis melaminium pentate and of hedric oxide ('"C~iARGUARD
329"')x"
Petrolatum TM 50.00 ('"PETROLATUM
RPB"'T
Granulated 100.00 hydrated sodium silicate ('"EXPANTROL
2")'"' Example 20 was prepared as described for Examples 1 and 2. The batch size was about 439 grams.
The expansion ratio of Example -20 was determined (as described in Examples 1 and 2) to be 7.05. The softness value was determined as described above under the heading "Softness Value Measurement" to be 5.6 mm.
The flow characteristic of the putty was good.
Example 20 passed both the "Flame Through Test"
and the "Fire Hose Stream Test.."
Example 21 The ingredients for Example 21 are listed in Table ~7, below.
Table 7 Amount of ' Ingredieats PHR*
Ingredient Example 21 tlnvulcaaised styrene 74.02 butadiene rubber ("AMERIPOL SYNPOL 8109"ITM
Styzene butadiene rubber 22.11 ("Polysar S
1018") ""
Moderately crosslinked 3.8?
butyl rubber ( POLYSAR XL 68102")'"' Thiodiethylene bas-(3,5-di-tart- 3.32 butyl-4-hydroxy) hydrocinnamate ("IRGANOX 1035")T""
Flamed silica ("CAB-O-SIL"!~" 14.3?
E ox resin owder ("SCOTCHCAST 16.59 265" T""
Powdered iron oxide ( 5. 53 F'e203 ) ( "IRON
OXIDE BF-1")'~"
Melamine oWder ("HERO 55.29 MELAMINE")T""
Boron Oxide Anhydrous 44.23 ("BORIC OXIDE
60 MESH)T""
Milled filaments ("MFX-1/8'TM 33.1?
IN") Iaobutylene butane copolymer 44.23 liqisid ( "INDOPOL H 100" )T""
Petrolatum ("PENRECO AMBER")TM- 66.34 Granulated hydrated sodium 132.68 silicate "EXPANTROL 4B~" ) r''"
Parts pu hundred based on the fatal robber and unvulcaaized rubber cf the pnay. ' The ingredients were compounded using the internal mixer described in Example 1.
The unwlcanized rubber ("Ameripol Synpol 810?N),M
and rubbers ("Polysar S 1018" and "POLYSAR BUTYL XL
68102~') were added to the mixing chamber of the mixer and then blended for about 6 minutes at about 60 rpm.
2o The speed of the mixing blades was then reduced to 90 rpm, and the antioxidant (i.e., thiodiethylene bis-(3,5-di-tart-butyl-4-hydroxy) hydrocinnamate), fumed silica, epoxy resin, iron oxide, boric oxide, melamine, s and milled glass fibers were added while mixing continued. The ingredients were mixed for about 3 minutes, after which the mixing speed was increased to . about 60 rpm. The plasticizes ("INDOPOL H-100")'was then added, and mixing continued for about 13 minutes.
The petrolatum was then slowly added and mixed in for about 5 minutes. Finally, the hydrated sodium silicate was added and mixed in for about 5 minutes. The bhtch size was about 466.44 grams.
The softness value of the putty, as determined is using the method described above under the heading "Softness Value Measurement"',was 6.32 mm. The expansion ratio of Example 21,, based on an average of two determinations, was 2.76. The flow characteristic of the putty. was excellent. ,'E~rther, the '"Flame 2o Through Test"' and the '"Fire Hose Stream Test."' Various modifications and alterations of this invention will become apparent to those skilled in the art without departing from the scope and spirit of this 25 invention. and it should be understood that this invention is not to be unduly limited to the illustrative embodiments set forth herein.
Claims (17)
1. ~An intumescent putty that remains soft and handleable for at least a month under ambient conditions comprising a blend of intumescent material, vulcanized rubber, and unvulcanized rubber, said vulcanized rubber and said unvulcanized rubber together providing said putty with a softness value of at least 4 mm, wherein measurement of the softness of the putty is described in ASTM D-1403-91, containing less than 0.25 percent by weight halogen, said putty containing less than 0.25 percent by weight water other than bound water, wherein bound water is water that does not come off until the putty is heated to at least 100°C, and said putty containing less than 0.25 percent by weight rubber curing agent, based on the total weight of the putty.
2. ~The putty according to claim 1 wherein said bound water is water that does not come off until the putty is heated to at least 150°C.
3. ~The putty according to claim 1 wherein said bound water is water that does not come off until the putty is heated to at least 250°C.
4. ~The putty according to claim 3 wherein said vulcanized rubber is selected from the group consisting of natural rubber, butyl rubbers, polybutadiene rubbers, synthetic isoprene rubbers, styrene butadiene rubbers, ethylene acrylic rubbers, nitrile rubbers, urethane rubbers, ethylene vinyl acetate rubbers, and combinations thereof, and said unvulcanized rubber is selected from the group consisting of unvulcanized natural rubber, unvulcanized butyl rubbers, unvulcanized polybutadiene rubbers, unvulcanized synthetic isoprene rubbers, unvulcanized styrene butadiene rubbers, unvulcanized ethylene acrylic rubbers, unvulcanized nitrile rubbers, unvulcanized urethane rubbers, unvulcanized ethylene vinyl acetate rubbers, and combinations thereof.
5. ~The putty according to claim 4 wherein said putty comprises about 10 to about 50 percent by weight of said unvulcanized rubber, based on the total weight of said putty.
6. ~The putty according to claim 5 wherein said putty comprises about 50 to about 200 percent by weight of said intumescent material, based on the total vulcanized rubber and unvulcanized rubber content of said putty.
7. ~The putty according to claim 4 wherein said putty further comprises a plasticizer, a char forming resin, a filler, and at least one of an antioxidant or an antiozonant.
8. ~The putty according to claim 4 wherein said putty further comprises a flame retardant, a plasticizer, a char forming resin, a filler, and at least one of an antioxidant or an antiozonant.
9. ~The putty according to claim 8 wherein said flame retardant is boric oxide.
10. ~The putty according to claim 4 wherein said putty having a softness value of at least 4.5 mm.
11. The putty according to claim 4 wherein said putty having a softness value of at leapt 5 mm.
12. The putty according to claim 4 wherein said putty having a softness value of at least 6 mm.
13. ~The putty according to claim 4 wherein said intumescent material is hydrated sodium silicate, and said putty further comprises a silicate fluxing agent.
14. ~The putty according to claim 4 wherein said intumescent material comprises graphite.
15. ~The putty according to claim 3 wherein said unvulcanized rubber is styrene butadiene rubber.
16. ~The putty according to any one of claims 1 to 15 comprising at least 5 percent by weight unvulcanized rubber, based on the total weight of the putty.
17. ~The putty according to any one of claims 1 to 15 comprising at least 10 percent by weight unvulcanized rubber, based on the total weight of the putty.
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US36695994A | 1994-12-30 | 1994-12-30 | |
| US08/366959 | 1994-12-30 | ||
| US08/567,956 | 1995-12-06 | ||
| US08/567,956 US5578671A (en) | 1994-12-30 | 1995-12-06 | Intumescent putty |
| PCT/US1995/016633 WO1996020987A1 (en) | 1994-12-30 | 1995-12-19 | Intumescent putty |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2208602A1 CA2208602A1 (en) | 1996-07-11 |
| CA2208602C true CA2208602C (en) | 2006-02-21 |
Family
ID=35929923
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002208602A Expired - Fee Related CA2208602C (en) | 1994-12-30 | 1995-12-19 | Intumescent putty |
Country Status (1)
| Country | Link |
|---|---|
| CA (1) | CA2208602C (en) |
-
1995
- 1995-12-19 CA CA002208602A patent/CA2208602C/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| CA2208602A1 (en) | 1996-07-11 |
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