Patent Application
20230130450
The present disclosure relates to methods of melt blending, and more specifically, to methods of melt blending flame retardant and polymeric compositions.
Polymeric compositions comprising halogenated flame-retardants are known. Examples of halogenated flame retardants include polymeric brominated flame retardants. Polymeric brominated flame retardants are known to face challenges when used with polyolefin flame retardant technology for wire and cable applications, because most of the commercially available polymeric brominated flame retardants are not polyolefins. The challenges arise due to differences in surface chemistry and polarity between the polymeric brominated flame retardants and the polyolefin as well as additives that may be utilized in the polyolefin. Further, the rather high molecular weights of polymeric brominated flame retardants can also present issues. Additionally, some polymeric brominated flame retardants exhibit glass transition temperatures or softening points that are higher than typical melting points of polyolefins, which can be problematic for melt mixing. In addition to compatibility issues, polymeric brominated flame retardants often have low thermal stability. The low thermal stability may result in premature thermal decomposition while melt blending with polyolefins to make formulated compounds (to use as flame retardant masterbatches) and/or during melt blending/extrusion with polyolefins to make coated conductors (i.e., insulated wires), thus leading to poor quality wires with associated loss of flame retardancy properties.
The issues facing the processing of polymeric brominated flame retardants are particularly troublesome as melt blending is a standard technique for combining the components of a polymeric composition. Melt blending involves both heating and mechanical agitation of the ingredients to produce a consistent melt blend of the polymeric composition. Melt blending is often performed by combining all of the ingredients of a polymeric composition at once while providing heating and mechanical agitation (“single-step melt blending”). Single-step melt blending is advantageous as it decreases the labor, complexity and time associated with forming polymeric compositions.
In view of the known incompatibilities of polymeric brominated flame retardants with polyolefins and the manufacturing efficiency associated with single step melt blending, it would be surprising to discover a useful multi-step method of melt blending a polymeric brominated flame retardant and polyolefin to form a flame retardant composition that enables the formation of coated conductors that pass a VW-1 Burn Test and a Horizontal Burn Test.
The present invention provides a useful multi-step method of melt blending a polymeric brominated flame retardant and polyolefin to form a flame-retardant composition that enables the formation of coated conductors that pass a VW-1 Burn Test and a Horizontal Burn Test.
The inventors of the present application have surprisingly discovered that in order to obtain sufficient dispersion of a polymeric brominated flame retardant in a polyolefin via melt blending the polymeric flame retardant must first be heated to a temperature above its glass transition temperature and then the polyolefin must be mixed in to form a homogenous melt before the addition of additives. The inventors have discovered that the polymeric brominated flame retardant, when processed with a polyolefin and other additives in single-step melt blending (or even following a multi-step sequence taught in the prior art), is not evenly dispersed in the polyolefin under non-destructive processing conditions. Simply performing the single-step melt blending for a longer period of time is not a solution because it risks causing degradation to the polyolefin and/or the polymeric brominated flame retardant. The inhomogeneity of the combined polymeric brominated flame retardant and polyolefin is carried over to coated conductors made from the combination resulting in failure of VW-1 and Horizontal Burn Tests. Surprisingly, flame retardant compositions having undergone single step melt blending (or multi-step blending of the prior art) are unable to produce coated conductors that can pass the VW-1 and Horizontal Burn Tests despite having similar compositions and mixing times as those of the surprising multi-step method.
The method of the present invention is particularly useful for forming polymeric compositions that can be used to form coated conductors, after combining with silane functionalized polyolefins and other additives and crosslinking by moisture cure.
According to a first feature of the present disclosure, a method of melt blending a flame-retardant composition, comprises the steps: (a) heating a polymeric brominated flame retardant to a temperature of 5° C. or greater above the polymeric brominated flame retardant's glass transition temperature as measured by Differential Scanning calorimetry, wherein the polymeric brominated flame retardant has a Temperature of 5% Mass Loss from 300° C. to 700° C. as measured according to Thermogravimetric Analysis; (b) mixing a polyolefin into the polymeric brominated flame retardant after step (a); and (c) mixing an inorganic filler into the polyolefin and polymeric brominated flame retardant after step (b) to form the flame-retardant composition.
According to a second feature of the present disclosure, the inorganic filler is selected from the group consisting of antimony trioxide, zinc borate, zinc carbonate, zinc carbonate hydroxide, hydrated zinc borate, zinc phosphate, zinc stannate, zinc hydrostannate, zinc sulfide, zinc oxide and combinations thereof.
According to a third feature of the present disclosure, the polyolefin has a crystallinity at 23° C. of from 0 wt % to 80 wt % as measured according to Crystallinity Testing.
According to a fourth feature of the present disclosure, the polymeric brominated flame retardant comprises aromatically brominated polystyrene.
According to a fifth feature of the present disclosure, the polymeric brominated flame retardant has a molecular weight of 1,000 g/mol to 20,000 g/mol as measured using gel permeation chromatography.
According to a sixth feature of the present disclosure, the polymeric brominated flame retardant has a molecular weight of 3,000 g/mol to 10,000 g/mol as measured using gel permeation chromatography.
According to a seventh feature of the present disclosure, step (a) further comprises heating the polymeric brominated flame retardant to a temperature of 160° C. to 220° C.
According to an eighth feature of the present disclosure, the polymeric brominated flame retardant has a Temperature of 5% Mass Loss from 300° C. to 400° C. as measured according to Thermogravimetric Analysis.
According to a ninth feature of the present disclosure, a method of forming a polymeric composition, comprises the step of: mixing the flame-retardant composition of any of features 1-8 with a silane functionalized ethylene polymer to form the polymeric composition.
According to a tenth feature of the present disclosure, a coated conductor comprises a conductor; and the polymeric composition produced by the method of feature 9 disposed at least partially around the conductor, wherein the coated conductor passes at least one of a VW-1 Burn Test and a Horizontal Burn Test.
As used herein, the term “and/or,” when used in a list of two or more items, means that any one of the listed items can be employed by itself, or any combination of two or more of the listed items can be employed. For example, if a composition is described as containing components A, B, and/or C, the composition can contain A alone; B alone; C alone; A and B in combination; A and C in combination; B and C in combination; or A, B, and C in combination.
All ranges include endpoints unless otherwise stated.
Test methods refer to the most recent test method as of the priority date of this document unless a date is indicated with the test method number as a hyphenated two-digit number. References to test methods contain both a reference to the testing society and the test method number. Test method organizations are referenced by one of the following abbreviations: ASTM refers to ASTM International (formerly known as American Society for Testing and Materials); EN refers to European Norm; DIN refers to Deutsches Institut für Normung; and ISO refers to International Organization for Standards.
As used herein, the term weight percent (“wt %”) designates the percentage by weight a component is of a total weight of the polymeric composition unless otherwise indicated.
As used herein, a “CAS number” is the chemical services registry number assigned by the Chemical Abstracts Service.
The present disclosure is directed to a method of melt blending a flame-retardant composition. The method comprises steps of (a) heating a polymeric brominated flame retardant (“PBFR”), (b) mixing a polyolefin into the polymeric brominated flame retardant after step (a); and (c) mixing an inorganic filler into the polyolefin and polymeric brominated flame retardant after step (b) to form the flame-retardant composition.
The present disclosure is also directed to a method of making a polymeric composition. The method of making the polymeric composition comprises mixing the flame-retardant composition with a silane-functionalized ethylene polymer to form the polymeric composition. The polymeric composition may be disposed at least partially around a conductor to form a coated conductor.
The method of melt blending the flame-retardant composition starts with heating the PBFR. The PBFR may be heated in a variety of manners. For example, the PBFR may be heated in a mixing bowl of a mixer, heated prior to being placed in a mixing bowl, heated in an extruder or pelletizer, or through other means. The PBFR is heated to a to a temperature of 5° C. or greater above the PBFR's glass transition temperature as measured by Differential Scanning calorimetry as described in greater detail below. For example, the PBFR may be heated to a temperature of 5° C. or greater, or 10° C. or greater, or 20° C. or greater, or 30° C. or greater, or 40° C. or greater, or 50° C. or greater, or 60° C. or greater, or 70° C. or greater, or 80° C. or greater, or 90° C. or greater, while at the same time, 100° C. or less, or 90° C. or less, or 80° C. or less, or 70° C. or less, or 60° C. or less, or 50° C. or less, or 40° C. or less, or 40° C. or less, or 30° C. or less, or 20° C. or less, or 10° C. or less than the glass transition temperature of the PBFR. The PBFR may be heated to a temperature of 160° C. or greater, or 170° C. or greater, or 180° C. or greater, or 190° C. or greater, or 200° C. or greater, or 210° C. or greater, while at the same time, 220° C. or less, or 210° C. or less, or 200° C. or less, or 190° C. or less, or 180° C. or less, or 170° C. or less.
The PBFR may have a Temperature of 5% Mass Loss from 300° C. to 700° C. as measured according to Thermogravimetric Analysis as explained below. The Temperature of 5% Mass Loss of the PBFR may be 300° C. or greater, or 310° C. or greater, or 320° C. or greater or 330° C. or greater, or 340° C. or greater, or 350° C. or greater, or 360° C. or greater, or 370° C. or greater, or 380° C. or greater, or 390° C. or greater, or 400° C. or greater, or 410° C. or greater, or 420° C. or greater, or 430° C. or greater, or 440° C. or greater, or 450° C. or greater, or 460° C. or greater, or 470° C. or greater, or 480° C. or greater, or 490° C. or greater, or 500° C. or greater, or 510° C. or greater, or 520° C. or greater, or 530° C. or greater, or 540° C. or greater, or 550° C. or greater, or 560° C. or greater, or 570° C. or greater, or 580° C. or greater, or 590° C. or greater, or 600° C. or greater, or 610° C. or greater, or 620° C. or greater, or 630° C. or greater, or 640° C. or greater, or 650° C. or greater, or 660° C. or greater, or 670° C. or greater, or 680° C. or greater, or 690° C. or greater, while at the same time, 700° C. or less, or 690° C. or less, or 680° C. or less, or 670° C. or less, or 660° C. or less, or 650° C. or less, or 640° C. or less, or 630° C. or less, or 620° C. or less, or 610° C. or less, 600° C. or less, or 590° C. or less, or 580° C. or less, or 570° C. or less, or 560° C. or less, or 550° C. or less, or 540° C. or less, or 530° C. or less, or 520° C. or less, or 510° C. or less, 500° C. or less, or 490° C. or less, or 480° C. or less, or 470° C. or less, or 460° C. or less, or 450° C. or less, or 440° C. or less, or 430° C. or less, or 420° C. or less, or 410° C. or less, or 400° C. or less, or 390° C. or less, or 380° C. or less, or 370° C. or less, or 360° C. or less, or 350° C. or less, or 340° C. or less, or 330° C. or less, or 320° C. or less, or 310° C. or less as measured according to Thermogravimetric Analysis. The Temperature of 5% Mass Loss is correlated with dehydrobromination of the PBFR. Premature dehydrobromination negatively affects the flame retardancy and as such having a Temperature of 5% Mass Loss from 300° C. to 700° C. is advantageous in increasing flame retardancy.
The PBFR may have a Retained Mass at 650° C. of 0 wt % to 50 wt % as measured according to Thermogravimetric Analysis as explained below. The PBFR may have a Retained Mass at 650° C. of 0 wt % or greater, or 1 wt % or greater, or 2 wt % or greater, or 5 wt % or greater, or 10 wt % or greater, or 13 wt % or greater, or 15 wt % or greater, or 18 wt % or greater, or 20 wt % or greater, or 25 wt % or greater, or 30 wt % or greater, or 35 wt % or greater, or 40 wt % or greater, or 45 wt % or greater, while at the same time, 50 wt % or less, or 45 wt % or less, or 40 wt % or less, or 35 wt % or less, or 30 wt % or less, or 25 wt % or less, or 20 wt % or less, or 18 wt % or less, or 15 wt % or less, or 13 wt % or less, or 10 wt % or less, or 5 wt % or less, or 4 wt % or less, or 3 wt % or less, or 1 wt % or less. The Retained Mass at 650° C. is an indication of the PBFR's ability to form char, which is often a carbonaceous material that insulates the material being protected, slowing pyrolysis and creating a barrier that hinders diffusion of oxygen/air as well as the vaporization of additional fuel gases generated by pyrolysis of polymeric composition into combustion zone. Thus, in terms of the well-known fire triangle, the formation of char is critically important to impart flame retardance as it both reduces heat transmission and slows down fire propagation.
The PBFR may be aromatically brominated. As used herein, the term “aromatically brominated” refers to the bonding of the bromine to aromatic moieties of the PBFR as opposed to aliphatic moieties. In a specific example, the PBFR may be aromatically brominated polystyrene. An example of an aromatically brominated polystyrene has a CAS number of 88497-56-7 and is commercially available under the tradename SAYTEX™ HP-3010 from Albemarle, Charlotte, N.C., USA. Aromatically brominated polystyrene has a bromine content of 68.5 wt %.
The PBFR may have a weight average molecular weight of from 1,000 grams per mol (g/mol) to 30,000 g/mol as measured using Gel Permeation Chromatography. For example, the weight average molecular weight of the PBFR may be 1,000 g/mol or greater, or 2,000 g/mol or greater, or 3,000 g/mol or greater, or 4,000 g/mol or greater, or 6,000 g/mol or greater, or 8,000 g/mol or greater, or 10,000 g/mol or greater, or 12,000 g/mol or greater, or 14,000 g/mol or greater, or 16,000 g/mol or greater, or 18,000 g/mol or greater, or 20,000 g/mol or greater, or 22,000 g/mol or greater, or 24,000 g/mol or greater, or 26,000 g/mol or greater, or 28,000 g/mol or greater, while at the same time, 30,000 g/mol or less, or 28,000 g/mol or less, or 26,000 g/mol or less, or 24,000 g/mol or less, or 22,000 g/mol or less, or 20,000 g/mol or less, or 18,000 g/mol or less, or 16,000 g/mol or less, or 14,000 g/mol or less, or 12,000 g/mol or less, or 10,000 g/mol or less, or 8,000 g/mol or less, or 6,000 g/mol or less, or 4,000 g/mol or less, or 2,000 g/mol or less as measured using gel permeation chromatography.
The PBFR may be utilized in such quantities that when the flame-retardant composition is incorporated in the polymeric composition, the polymeric composition may comprise from 5 wt % to 50 wt % of the brominated flame retardant based on the total weight of the polymeric composition. For example, the polymeric composition may comprise 5 wt % or greater, 10 wt % or greater, 11 wt % or greater, or 13 wt % or greater, or 15 wt % or greater, or 20 wt % or greater, or 25 wt % or greater, or 30 wt % or greater, or 31 wt % or greater, or 32 wt % or greater, or 33 wt % or greater, or 34 wt % or greater, or 35 wt % or greater, or 36 wt % or greater, or 37 wt % or greater, or 38 wt % or greater, or 39 wt % or greater, or 40 wt % or greater, or 41 wt % or greater, or 42 wt % or greater, or 43 wt % or greater, or 44 wt % or greater, or 45 wt % or greater, or 46 wt % or greater, or 47 wt % or greater, or 48 wt % or greater, or 49 wt % or greater, while at the same time, 50 wt % or less, or 49 wt % or less, or 48 wt % or less, or 47 wt % or less, or 46 wt % or less, or 45 wt % or less, or 44 wt % or less, or 43 wt % or less, or 42 wt % or less, or 41 wt % or less, or 40 wt % or less, or 39 wt % or less, or 38 wt % or less, or 37 wt % or less, or 36 wt % or less, or 35 wt % or less, or 34 wt % or less, or 33 wt % or less, or 32 wt % or less, or 31 wt % or less, or 30 wt % or less, or 25 wt % or less, or 20 wt % or less, or 15 wt % or less, or 13 wt % or less, or 11 wt % or less, or 10 wt % or less of the PBFR based on a total weight of the polymeric composition.
Step (b) includes mixing a polyolefin into the PBFR after step (a). As explained above, the conventional use of PBFRs in polyethylene chemistry has been fraught with challenge due to the differences in surface chemistry, molecular weight, high glass transition temperatures and low thermal stability that all affect the ability to melt blend PBFR and a polyolefin. The inventors of the present application have surprisingly discovered that by utilizing a specific multistep melt blending method, certain PBFRs may be mixed with polyolefins to form flame retardant compositions that can be used to form polymeric compositions. The inventors have discovered that the PBFR must be heated to a temperature above its glass transition temperature (i.e., step (a)) before step (b) of mixing the polyolefin into the PBFR can be performed. By utilizing the correct PBFR and “softening” the PBFR first, the polyolefin can be mixed into the PBFR (1) homogeneously enough to evenly disperse the PBFR and (2) with sufficiently low mixing to prevent damage (i.e., debromination and/or degradation) form occurring to the PBFR and/or the polyolefin.
The polyolefin comprises polymerized α-olefins and optionally unsaturated esters. The α-olefin may include C2, or C3 to C4, or C6, or C8, or C10, or C12, or C16, or C18, or C20 α-olefins, such as ethylene, propylene, 1-butene, 1-hexene, 4-methyl-1-pentene, and 1-octene. The unsaturated esters can be alkyl acrylates, alkyl methacrylates, or vinyl carboxylates. The polyolefin may have a crystallinity at 23° C. from 0 wt % to 80 wt % as measured according to Crystallinity Testing as provided below. For example, the crystallinity at 23° C. of the polyolefin may be 0 wt % or greater, or 5 wt % or greater, or 10 wt % or greater, or 15 wt % or greater, or 20 wt % or greater, or 25 wt % or greater, or 30 wt % or greater, or 35 wt % or greater, or 40 wt % or greater, or 45 wt % or greater, or 50 wt % or greater, or 55 wt % or greater, or 60 wt % or greater, or 65 wt % or greater, or 70 wt % or greater, or 75 wt % or greater, while at the same time, 80 wt % or less, or 75 wt % or less, or 70 wt % or less, or 65 wt % or less, or 60 wt % or less, or 55 wt % or less, or 50 wt % or less, or 45 wt % or less, or 40 wt % or less, or 35 wt % or less, or 30 wt % or less, or 25 wt % or less, or 20 wt % or less, or 15 wt % or less, or 10 wt % or less as measured according to Crystallinity Testing.
The polyolefin may be an ultra-low-density polyethylene or a linear low-density polyethylene or a high-density polyethylene or an ethylene ethyl acrylate copolymer or an ethylene vinyl acetate copolymer. The density of the polyolefin may be 0.860 g/cc or greater, or 0.870 g/cc or greater, or 0.880 g/cc or greater, or 0.890 g/cc or greater, or 0.900 g/cc or greater, or 0.904 g/cc or greater, or 0.910 g/cc or greater, or 0.915 g/cc or greater, or 0.920 g/cc or greater, or 0.921 g/cc or greater, or 0.922 g/cc or greater, or 0.925 g/cc to 0.930 g/cc or greater, or 0.935 g/cc or greater, while at the same time, 0.970 g/cc or less, or 0.960 g/cc or less, or 0.950 g/cc or less, or 0.940 g/cc or less, or 0.935 g/cc or less, or 0.930 g/cc or less, or 0.925 g/cc or less, or 0.920 g/cc or less, or 0.915 g/cc or less, or 0.910 g/cc or less, or 0.905 g/cc or less, or 0.900 g/cc or less as measured according to ASTM D792.
The polyolefin has a melt index as measured according to ASTM D1238 under the conditions of 190° C./2.16 kilogram (kg) weight and is reported in grams eluted per 10 minutes (g/10 min). The melt index of the polyolefin may be 0.5 g/10 min or greater, or 1.0 g/10 min or greater, or 1.5 g/10 min or greater, or 2.0 g/10 min or greater, or 2.5 g/10 min or greater, or 3.0 g/10 min or greater, or 3.5 g/10 min or greater, or 4.0 g/10 min or greater, or 4.5 g/10 min or greater, while at the same time, 30.0 g/10 min or less, or 25.0 g/10 min or less, or 20.0 g/10 min or less, or 15.0 g/10 min or less, or 10.0 g/10 min or less, or 5.0 g/10 min or less, or 4.5 g/10 min or less, or 4.0 g/10 min or less, or 3.5 g/10 min or less, or 3.0 g/10 min or less, or 2.5 g/10 min or less, or 2.0 g/10 min or less, or 1.5 g/10 min or less, or 1.0 g/10 min or less.
The polyolefin may be utilized in such quantities that when the flame-retardant composition is incorporated in the polymeric composition, the polymeric composition may comprise from 0 wt % to 30 wt % of second polyolefin based on the total weight of the polymeric composition. The polymeric composition may comprise 0 wt % or greater, or 5 wt % or greater, or 10 wt % or greater, or 15 wt % or greater, or 20 wt % or greater, or 25 wt % or greater, while at the same time, 30 wt % or less, or 25 wt % or less, or 20 wt % or less, or 15 wt % or less, or 10 wt % of the polyolefin.
Step (c) includes mixing an inorganic filler into the polyolefin and polymeric brominated flame retardant after step (b) to form the flame-retardant composition. The inorganic filler is selected from the group consisting of the group consisting of antimony trioxide, zinc borate, zinc carbonate, zinc carbonate hydroxide, hydrated zinc borate, zinc phosphate, zinc stannate, zinc hydrostannate, zinc sulfide, zinc oxide and combinations thereof.
Antimony trioxide (Sb2O3) has the CAS number 1309-64-4 and the following Structure (II):
Antimony trioxide has a molecular weight (Mw) of 291.518 grams per mole (g/mol). One gram of antimony trioxide (Sb2O3) contains 0.835345774 grams antimony (Sb). Antimony trioxide is commercially available under the tradename MICROFINE™ A09 from Great Lakes Solution, and BRIGHTSUN™ HB from China Antimony Chemicals Co., Ltd. The antimony trioxide may be utilized in such quantities that when the flame-retardant composition is incorporated in the polymeric composition, the polymeric composition may comprise 5 wt % to 50 wt % of the antimony trioxide based on the total weight of the polymeric composition. For example, the polymeric composition may comprise 5 wt % or greater, 10 wt % or greater, 11 wt % or greater, or 13 wt % or greater, or 15 wt % or greater, or 20 wt % or greater, or 25 wt % or greater, or 30 wt % or greater, or 31 wt % or greater, or 32 wt % or greater, or 33 wt % or greater, or 34 wt % or greater, or 35 wt % or greater, or 36 wt % or greater, or 37 wt % or greater, or 38 wt % or greater, or 39 wt % or greater, or 40 wt % or greater, or 41 wt % or greater, or 42 wt % or greater, or 43 wt % or greater, or 44 wt % or greater, or 45 wt % or greater, or 46 wt % or greater, or 47 wt % or greater, or 48 wt % or greater, or 49 wt % or greater, while at the same time, 50 wt % or less, or 49 wt % or less, or 48 wt % or less, or 47 wt % or less, or 46 wt % or less, or 45 wt % or less, or 44 wt % or less, or 43 wt % or less, or 42 wt % or less, or 41 wt % or less, or 40 wt % or less, or 39 wt % or less, or 38 wt % or less, or 37 wt % or less, or 36 wt % or less, or 35 wt % or less, or 34 wt % or less, or 33 wt % or less, or 32 wt % or less, or 31 wt % or less, or 30 wt % or less, or 25 wt % or less, or 20 wt % or less, or 15 wt % or less, or 13 wt % or less, or 11 wt % or less, or 10 wt % or less of the antimony trioxide based on a total weight of the polymeric composition.
The flame retardant composition may include one or more zinc flame retardant synergists. As used herein, a “flame retardant synergist” is a compound that increases the flame retardancy properties of a flame retardant. Zinc flame retardant synergists may include zinc borate, zinc carbonate, zinc carbonate hydroxide, hydrated zinc borate, zinc phosphate, zinc stannate, zinc hydrostannate, zinc sulfide and zinc oxide. One example of a zinc oxide flame retardant synergist is commercially available as FIREBRAKE™ ZB-fine from Rio Tinto, London, England.
The zinc flame retardant synergist may be utilized in such quantities that when the flame-retardant composition is incorporated in the polymeric composition, the polymeric composition may comprise 0 wt % or greater, or 0.5 wt % or greater, or 1 wt % or greater, or 2 wt % or greater, or 3 wt % or greater, or 4 wt % or greater, or 5 wt % or greater, or 6 wt % or greater, or 7 wt % or greater, or 8 wt % or greater, or 9 wt % or greater, or 10 wt % or greater, or 11 wt % or greater, or 12 wt % or greater, or 13 wt % or greater, or 14 wt % or greater, while at the same time, 15 wt % or less, or 14 wt % or less, or 13 wt % or less, or 12 wt % or less, or 11 wt % or less, or 10 wt % or less, or 9 wt % or less, or 8 wt % or less, or 7 wt % or less, or 6 wt % or less, or 5 wt % or less, or 4 wt % or less, or 3 wt % or less, or 2 wt % or less, or 1 wt % or less of more zinc flame retardant synergists.
As stated above, the flame-retardant composition may be utilized to form the polymeric composition. For example, the method of making the polymeric composition comprises mixing the flame-retardant composition with a silane functionalized ethylene polymer to form the polymeric composition.
A “silane-functionalized polyolefin” is a polymer that contains silane and equal to or greater than 50 wt %, or a majority amount, of polymerized α-olefin, based on the total weight of the silane-functionalized polyolefin. “Polymer” means a macromolecular compound prepared by reacting (i.e., polymerizing) monomers of the same or different type. As noted above, the polymeric composition comprises the silane-functionalized polyolefin. The silane-functionalized polyolefin crosslinks typically in the presence of moisture with suitable catalyst at elevated temperature and in doing so increases the resistance to flow of the polymeric composition.
The silane-functionalized polyolefin may include an α-olefin and silane copolymer, a silane-grafted polyolefin, and/or combinations thereof. An “α-olefin and silane copolymer” (α-olefin/silane copolymer) is formed from the copolymerization of an α-olefin (such as ethylene) and a hydrolyzable silane monomer (such as a vinyl silane monomer) such that the hydrolyzable silane monomer is incorporated into the backbone of the polymer chain prior to the polymer's incorporation into the polymeric composition. A “silane-grafted polyolefin” or “Si-g-PO” may be formed by the Sioplas process in which a hydrolyzable silane monomer is grafted onto the backbone of a base polyolefin by a process such as extrusion, prior to the polymer's incorporation into the polymeric composition.
In examples where the silane-functionalized polyolefin is an α-olefin and silane copolymer, the silane-functionalized polyolefin is prepared by the copolymerization of at least one α-olefin and a hydrolyzable silane monomer. In examples where the silane-functionalized polyolefin is a silane grafted polyolefin, the silane-functionalized polyolefin is prepared by grafting one or more hydrolyzable silane monomers on to the polymerized α-olefin backbone of a polymer.
The silane-functionalized polyolefin may comprise 50 wt % or greater, 60 wt % or greater, 70 wt % or greater, 80 wt % or greater, 85 wt % or greater, 90 wt % or greater, or 91 wt % or greater, or 92 wt % or greater, or 93 wt % or greater, or 94 wt % or greater, or 95 wt % or greater, or 96 wt % or greater, or 97 wt % or greater, or 97.5 wt % or greater, or 98 wt % or greater, or 99 wt % or greater, while at the same time, 99.5 wt % or less, or 99 wt % or less, or 98 wt % or less, or 97 wt % or less, or 96 wt % or less, or 95 wt % or less, or 94 wt % or less, or 93 wt % or less, or 92 wt % or less, or 91 wt % or less, or 90 wt % or less, or 85 wt % or less, or 80 wt % or less, or 70 wt % or less, or 60 wt % or less of α-olefin as measured using Nuclear Magnetic Resonance (NMR) or Fourier-Transform Infrared (FTIR) Spectroscopy. The α-olefin may include C2, or C3 to C4, or C6, or C8, or C10, or C12, or C16, or C18, or C20 α-olefins, such as ethylene, propylene, 1-butene, 1-hexene, 4-methyl-1-pentene, and 1-octene. Other units of the silane-functionalized polyolefin may be derived from one or more polymerizable monomers including, but not limited to, unsaturated esters. The unsaturated esters may be alkyl acrylates, alkyl methacrylates, or vinyl carboxylates. The alkyl groups can have from 1 to 8 carbon atoms, or from 1 to 4 carbon atoms. The carboxylate groups can have from 2 to 8 carbon atoms, or from 2 to 5 carbon atoms. Examples of acrylates and methacrylates include, but are not limited to, ethyl acrylate, methyl acrylate, methyl methacrylate, t-butyl acrylate, n-butyl acrylate, n-butyl methacrylate, and 2-ethylhexyl acrylate. Examples of vinyl carboxylates include, but are not limited to, vinyl acetate, vinyl propionate, and vinyl butanoate.
The silane-functionalized polyolefin has a density of 0.860 g/cc or greater, or 0.870 g/cc or greater, or 0.880 g/cc or greater, or 0.890 g/cc or greater, or 0.900 g/cc or greater, or 0.910 g/cc or greater, or 0.915 g/cc or greater, or 0.920 g/cc or greater, or 0.921 g/cc or greater, or 0.922 g/cc or greater, or 0.925 g/cc to 0.930 g/cc or greater, or 0.935 g/cc or greater, while at the same time, 0.970 g/cc or less, or 0.960 g/cc or less, or 0.950 g/cc or less, or 0.940 g/cc or less, or 0.935 g/cc or less, or 0.930 g/cc or less, or 0.925 g/cc or less, or 0.920 g/cc or less, or 0.915 g/cc or less as measured by ASTM D792.
A “hydrolyzable silane monomer” is a silane-containing monomer that will effectively copolymerize with an α-olefin (e.g., ethylene) to form an α-olefin/silane copolymer (such as an ethylene/silane copolymer), or graft to an α-olefin polymer (i.e., a polyolefin) to form a Si-g-polyolefin, thus enabling subsequent crosslinking of the silane-functionalized polyolefin. A representative, but not limiting, example of a hydrolyzable silane monomer has structure (I):
in which R1 is a hydrogen atom or methyl group; x is 0 or 1; n is an integer from 1 to 4, or 6, or 8, or 10, or 12; and each R2 independently is a hydrolyzable organic group such as an alkoxy group having from 1 to 12 carbon atoms (e.g., methoxy, ethoxy, butoxy), an aryloxy group (e.g., phenoxy), an araloxy group (e.g., benzyloxy), an aliphatic acyloxy group having from 1 to 12 carbon atoms (e.g., formyloxy, acetyloxy, propanoyloxy), an amino or substituted amino group (e.g., alkylamino, arylamino), or a lower-alkyl group having 1 to 6 carbon atoms, with the proviso that not more than one of the three R2 groups is an alkyl. The hydrolyzable silane monomer may be copolymerized with an α-olefin (such as ethylene) in a reactor, such as a high-pressure process, to form an α-olefin/silane copolymer. In examples where the α-olefin is ethylene, such a copolymer is referred to herein as an ethylene/silane copolymer. The hydrolyzable silane monomer may also be grafted to a polyolefin (such as a polyethylene) by the use of an organic peroxide, such as 2,5-bis(tert-butylperoxy)-2,5-dimethylhexane, to form a Si-g-PO or an in-situ Si-g-PO. The in-situ Si-g-PO is formed by a process such as the MONOSIL process, in which a hydrolyzable silane monomer is grafted onto the backbone of a polyolefin during the extrusion of the present composition to form a coated conductor, as described, for example, in U.S. Pat. No. 4,574,133.
The hydrolyzable silane monomer may include silane monomers that comprise an ethylenically unsaturated hydrocarbyl group, such as a vinyl, allyl, isopropenyl, butenyl, cyclohexenyl or gamma (meth)acryloxy allyl group, and a hydrolyzable group, such as, for example, a hydrocarbyloxy, hydrocarbonyloxy, or hydrocarbylamino group. Hydrolyzable groups may include methoxy, ethoxy, formyloxy, acetoxy, proprionyloxy, and alkyl or arylamino groups. In a specific example, the hydrolyzable silane monomer is an unsaturated alkoxy silane, which can be grafted onto the polyolefin or copolymerized in-reactor with an α-olefin (such as ethylene). Examples of hydrolyzable silane monomers include vinyltrimethoxysilane (VTMS), vinyltriethoxysilane (VTES), vinyltriacetoxysilane, and gamma-(meth)acryloxy propyl trimethoxy silane. In context to Structure (I), for VTMS: x=0; R1=hydrogen; and R2=methoxy; for VTES: x=0; R1=hydrogen; and R2=ethoxy; and for vinyltriacetoxysilane: x=0; R1=H; and R2=acetoxy.
Examples of suitable ethylene/silane copolymers are commercially available as SI-LINK™ DFDA-5451 NT and SI-LINK™ AC DFDB-5451 NT, each available from The Dow Chemical Company, Midland, Mich. Examples of suitable Si-g-PO are commercially available as PEXIDAN™ A-3001 from SACO AEI Polymers, Sheboygan, Wis. and SYNCURE™ S1054A from PolyOne, Avon Lake, Ohio.
The silane-functionalized polyolefin may be mixed with the flame-retardant composition in such quantities that the polymeric composition may comprise from 25 wt % to 75 wt % of silane-functionalized polyolefin. For example, the polymeric composition may comprise 25 wt % or greater, or 26 wt % or greater, or 28 wt % or greater, or 30 wt % or greater, or 32 wt % or greater, or 34 wt % or greater, or 36 wt % or greater, or 38 wt % or greater, or 40 wt % or greater, or 42 wt % or greater, or 44 wt % or greater, or 46 wt % or greater, or 48 wt % or greater, or 50 wt % or greater, or 52 wt % or greater, or 54 wt % or greater, or 56 wt % or greater, or 58 wt % or greater, or 60 wt % or greater, or 65 wt % or greater, or 70 wt % or greater, while at the same time, 75 wt % or less, or 70 wt % or less, or 65 wt % or less, or 60 wt % or less, or 58 wt % or less, or 56 wt % or less, or 54 wt % or less, or 52 wt % or less, or 40 wt % or less, or 48 wt % or less, or 46 wt % or less, or 44 wt % or less, or 42 wt % or less, or 40 wt % or less, or 38 wt % or less, or 36 wt % or less, or 34 wt % or less, or 32 wt % or less, or 30 wt % or less, or 28 wt % or less, or 26 wt % or less of silane-functionalized polyolefin based on a total weight of the polymeric composition.
The silane-functionalized polyolefin has a melt index as measured according to ASTM D1238 under the conditions of 190° C./2.16 kilogram (kg) weight and is reported in grams eluted per 10 minutes (g/10 min). The melt index of the silane functionalized polyolefin may be 0.5 g/10 min or greater, or 1.0 g/10 min or greater, or 1.5 g/10 min or greater, or 2.0 g/10 min or greater, or 2.5 g/10 min or greater, or 3.0 g/10 min or greater, or 3.5 g/10 min or greater, or 4.0 g/10 min or greater, or 4.5 g/10 min or greater, while at the same time, 30.0 g/10 min or less, or 25.0 g/10 min or less, or 20.0 g/10 min or less, or 15.0 g/10 min or less, or 10.0 g/10 min or less, or 5.0 g/10 min or less, or 4.5 g/10 min or less, or 4.0 g/10 min or less, or 3.5 g/10 min or less, or 3.0 g/10 min or less, or 2.5 g/10 min or less, or 2.0 g/10 min or less, or 1.5 g/10 min or less, or 1.0 g/10 min or less.
The polymeric composition may include one or more additives. The additives may be added in any one of steps (a), (b) and (c) of the method of melt blending the flame-retardant composition. The additives may be combined with either of or added separately from the flame-retardant composition and silane functionalized polyolefin when forming the polymeric composition. Nonlimiting examples of suitable additives include antioxidants, colorants, corrosion inhibitors, lubricants, silanol condensation catalysts, ultraviolet (UV) absorbers or stabilizers, anti-blocking agents, flame retardants, coupling agents, compatibilizers, plasticizers, fillers, processing aids, and combinations thereof.
The polymeric composition may include an antioxidant. Nonlimiting examples of suitable antioxidants include phenolic antioxidants, thio-based antioxidants, phosphate-based antioxidants, and hydrazine-based metal deactivators. Suitable phenolic antioxidants include high molecular weight hindered phenols, methyl-substituted phenol, phenols having substituents with primary or secondary carbonyls, and multifunctional phenols such as sulfur and phosphorous-containing phenol. Representative hindered phenols include 1,3,5-trimethyl-2,4,6-tris-(3,5-di-tert-butyl hydroxybenzyl)-benzene; pentaerythrityl tetrakis-3(3,5-di-tert-butyl-4-hydroxyphenyl)-propionate; n-octadecyl-3(3,5-di-tert-butyl-4-hydroxyphenyl)-propionate; 4,4′-methylenebis(2,6-tert-butyl-phenol); 4,4′-thiobis(6-tert-butyl-o-cresol); 2,6-di-tertbutylphenol; 6-(4-hydroxyphenoxy)-2,4-bis(n-octyl-thio)-1,3,5 triazine; di-n-octylthio)ethyl 3,5-di-tert-butyl hydroxy-benzoate; and sorbitol hexa[3-(3,5-di-tert-butyl-4-hydroxy-phenyl)-propionate]. In an embodiment, the composition includes pentaerythritol tetrakis(3-(3,5-di-tert-butyl hydroxyphenyl)propionate), commercially available as Irganox™ 1010 from BASF. A nonlimiting example of a suitable methyl-substituted phenol is isobutylidenebis(4,6-dimethylphenol). A nonlimiting example of a suitable hydrazine-based metal deactivator is oxalyl bis(benzylidiene hydrazide). In an embodiment, the composition contains from 0 wt %, or 0.001 wt %, or 0.01 wt %, or 0.02 wt %, or 0.05 wt %, or 0.1 wt %, or 0.2 wt %, or 0.3 wt %, or 0.4 wt % to 0.5 wt %, or 0.6 wt %, or 0.7 wt %, or 0.8 wt %, or 1.0 wt %, or 2.0 wt %, or 2.5 wt %, or 3.0 wt % antioxidant, based on total weight of the composition.
The polymeric composition may include a silanol condensation catalyst, such as Lewis and Brønsted acids and bases. A “silanol condensation catalyst” promotes crosslinking of the silane functionalized polyolefin through hydrolysis and condensation reactions. Lewis acids are chemical species that can accept an electron pair from a Lewis base. Lewis bases are chemical species that can donate an electron pair to a Lewis acid. Nonlimiting examples of suitable Lewis acids include the tin carboxylates such as dibutyl tin dilaurate (DBTDL), dimethyl hydroxy tin oleate, dioctyl tin maleate, di-n-butyl tin maleate, dibutyl tin diacetate, dibutyl tin dioctoate, stannous acetate, stannous octoate, and various other organo-metal compounds such as lead naphthenate, zinc caprylate and cobalt naphthenate. Nonlimiting examples of suitable Lewis bases include the primary, secondary and tertiary amines Nonlimiting examples of suitable Brønsted acids are methanesulfonic acid, benzenesulfonic acid, dodecylbenzenesulfonic acid, naphthalenesulfonic acid, or an alkylnaphthalenesulfonic acid. The silanol condensation catalyst may comprise a blocked sulfonic acid. The blocked sulfonic acid may be as defined in US 2016/0251535 A1 and may be a compound that generates in-situ a sulfonic acid upon heating thereof, optionally in the presence of moisture or an alcohol. Examples of blocked sulfonic acids include amine-sulfonic acid salts and sulfonic acid alkyl esters. The blocked sulfonic acid may consist of carbon atoms, hydrogen atoms, one sulfur atom, and three oxygen atoms, and optionally a nitrogen atom. These catalysts are typically used in moisture cure applications. The polymeric composition includes from 0 wt %, or 0.001 wt %, or 0.005 wt %, or 0.01 wt %, or 0.02 wt %, or 0.03 wt % to 0.05 wt %, or 0.1 wt %, or 0.2 wt %, or 0.5 wt %, or 1.0 wt %, or 3.0 wt %, or 5.0 wt %, or 10 wt % or 20 wt % silanol condensation catalyst, based on the total weight of the composition. The silanol condensation catalyst is typically added to the article manufacturing-extruder (such as during cable manufacture) so that it is present during the final melt extrusion process. As such, the silane functionalized polyolefin may experience some crosslinking before it leaves the extruder with the completion of the crosslinking after it has left the extruder, typically upon exposure to moisture (e.g., a sauna, hot water bath or a cooling bath) and/or the humidity present in the environment in which it is stored, transported or used.
The silanol condensation catalyst may be included in a catalyst masterbatch blend with the catalyst masterbatch being included in the composition. Nonlimiting examples of suitable catalyst masterbatches include those sold under the trade name SI-LINK™ from The Dow Chemical Company, including SI-LINK™ DI-DA-5481 Natural and SI-LINK™ AC DFDA-5488 NT. In an embodiment, the composition contains from 0 wt %, or 0.001 wt %, or 0.01 wt %, or 0.5 wt %, or 1.0 wt %, or 2.0 wt %, or 3.0 wt %, or 4.0 wt % to 5.0 wt %, or 6.0 wt %, or 7.0 wt %, or 8.0 wt %, or 9.0 wt %, or 10.0 wt %, or 15.0 wt %, or 20.0 wt % catalyst masterbatch, based on total weight of the composition.
The polymeric composition may include an ultraviolet (UV) absorber or stabilizer. A nonlimiting example of a suitable UV stabilizer is a hindered amine light stabilizer (HALS). A nonlimiting example of a suitable HALS is 1,3,5-Triazine-2,4,6-triamine, N,N-1,2-ethanediylbisN-3-4,6-bisbutyl(1,2,2,6,6-pentamethyl-4-piperidinyl) amino-1,3,5-triazin-2-ylaminopropyl-N,N-dibutyl-N,N-bis(1,2,2,6,6-pentamethyl-4-piperidinyl)-1,5,8,12-tetrakis[4,6-bis(n-butyl-n-1,2,2,6,6-pentamethyl-4-piperidylamino)-1,3,5-triazin-2-yl]-1,5,8,12-tetraazadodecane, which is commercially available as SABO™ STAB UV-119 from SABO S.p.A. of Levate, Italy. In an embodiment, the polymeric composition contains from 0 wt %, or 0.001 wt %, or 0.002 wt %, or 0.005 wt %, or 0.006 wt % to 0.007 wt %, or 0.008 wt %, or 0.009 wt %, or 0.01 wt %, or 0.2 wt %, or 0.3 wt %, or 0.4 wt %, or 0.5 wt %, 1.0 wt %, or 2.0 wt %, or 2.5 wt %, or 3.0 wt % UV absorber or stabilizer, based on total weight of the composition.
The polymeric composition may include a filler. Nonlimiting examples of suitable fillers include carbon black, organo-clay, aluminum trihydroxide, magnesium hydroxide, calcium carbonate, hydromagnesite, huntite, hydrotalcite, boehmite, magnesium carbonate, magnesium phosphate, calcium hydroxide, calcium sulfate, silica, silicone gum, talc and combinations thereof. The filler may or may not have flame retardant properties. In an embodiment, the filler is coated with a material that will prevent or retard any tendency that the filler might otherwise have to interfere with the silane cure reaction. Stearic acid is illustrative of such a filler coating. In an embodiment, the composition contains from 0 wt %, or 0.01 wt %, or 0.02 wt %, or 0.05 wt %, or 0.07 wt %, or 0.1 wt %, or 0.2 wt %, or 0.3 wt %, or 0.4 wt % to 0.5 wt %, or 0.6 wt %, or 0.7 wt %, or 0.8 wt %, or 1.0 wt %, or 2.0 wt %, or 2.5 wt %, or 3.0 wt %, or 5.0 wt %, or 8.0 wt %, or 10.0 wt %, or 20 wt % filler, based on total weight of the polymeric composition.
In an embodiment, the polymeric composition includes a processing aid. Nonlimiting examples of suitable processing aids include oils, polydimethylsiloxane, organic acids (such as stearic acid), and metal salts of organic acids (such as zinc stearate). In an embodiment, the composition contains from 0 wt %, or 0.01 wt %, or 0.02 wt %, or 0.05 wt %, or 0.07 wt %, or 0.1 wt %, or 0.2 wt %, or 0.3 wt %, or 0.4 wt % to 0.5 wt %, or 0.6 wt %, or 0.7 wt %, or 0.8 wt %, or 1.0 wt %, or 2.0 wt %, or 2.5 wt %, or 3.0 wt %, or 5.0 wt %, or 10.0 wt % processing aid, based on total weight of the polymeric composition.
In an embodiment, the polymeric composition contains from 0 wt %, or greater than 0 wt %, or 0.001 wt %, or 0.002 wt %, or 0.005 wt %, or 0.006 wt % to 0.007 wt %, or 0.008 wt %, or 0.009 wt %, or 0.01 wt %, or 0.2 wt %, or 0.3 wt %, or 0.4 wt %, or 0.5 wt %, 1.0 wt %, or 2.0 wt %, or 2.5 wt %, or 3.0 wt %, or 4.0 wt %, or 5.0 wt % to 6.0 wt %, or 7.0 wt %, or 8.0 wt %, or 9.0 wt %, or 10.0 wt %, or 15.0 wt %, or 20.0 wt %, or 30 wt %, or 40 wt %, or 50 wt % additive, based on the total weight of the polymeric composition.
The polymeric composition contains antimony trioxide and PBFR in such relative quantities that the antimony (Sb) and bromine (Br) is at a molar ratio (Sb:Br molar ratio) from 0.35 to 0.98. For example, the polymeric composition has a Sb:Br molar ratio of 0.35 or greater, or 0.40 or greater, or 0.45 or greater, or 0.50 or greater, or 0.55 or greater, or 0.60 or greater, or 0.65 or greater, or 0.70 or greater, or 0.75 or greater, or 0.80 or greater, or 0.85 or greater, or 0.90 or greater, or 0.95 or greater, while at the same time, 0.98 or less, or 0.95 or less, or 0.90 or less, or 0.85 or less, or 0.80 or less, or 0.75 or less, or 0.70 or less, or 0.65 or less, or 0.60 or less, or 0.55 or less, or 0.50 or less, or 0.45 or less, or 0.40 or less. The Sb:Br molar ratio is calculated in accordance with the following Equation (1):
The number of moles of antimony (Sb) in the polymeric composition from the antimony trioxide (Sb2O3) is calculated in accordance with the following Equation (1A):
wherein, the molecular weight of antimony trioxide is 291.52 g/mol.
The number of moles of bromine in the polymeric composition from the PBFR is calculated in accordance with the following Equation (1B):
wherein, the atomic weight of bromine is 79.904 g/mol.
The polymeric composition contains zinc flame retardant synergists and PBFR in such relative quantities that the zinc (Zn) and bromine (Br) are at a molar ratio (Zn:Br molar ratio) of 0.0, or greater than 0.0 to 0.185. For example, the Zn:Br molar ratio may be 0.010 or greater, or 0.020 or greater, or 0.030 or greater, or 0.040 or greater, or 0.050 or greater, or 0.060 or greater, or 0.070 or greater, or 0.080 or greater, or 0.090 or greater, or 0.100 or greater, or 0.110 or greater, or 0.120 or greater, or 0.130 or greater, or 0.140 or greater, or 0.150 or greater, or 0.160 or greater, or 0.170 or greater, or 0.180 or greater, while at the same time, 0.185 or less, or 0.180 or less, or 0.170 or less, or 0.160 or less, or 0.150 or less, or 0.140 or less, or 0.130 or less, or 0.120 or less, or 0.110 or less, or 0.100 or less, or 0.090 or less, or 0.080 or less, or 0.070 or less, or 0.060 or less, or 0.050 or less, or 0.040 or less, or 0.030 or less, or 0.020 or less, or 0.010 or less. The Zn:Br molar ratio is calculated in accordance with the following Equation (2):
The number of moles of bromine in the polymeric composition from the PBFR is calculated in accordance with the Equation (1B). The number of moles of zinc in the polymeric composition from the zinc flame retardant synergist is calculated in accordance with the following Equation (2A):
wherein, the molecular weight of zinc oxide is 81.406 g/mol. The moles of zinc oxide in the polymeric composition is equal to the moles of zinc oxide in the polymeric composition.
The grams of bromine within the polymeric composition can readily be determined from the amount of PBFR in the polymeric composition and the amount of bromine in the PBFR. The grams of zinc within the polymeric composition can readily be determined from the amount of zinc flame retardant synergist in the polymeric composition and the amount of zinc in the zinc flame retardant synergist.
The present disclosure also provides a coated conductor. The coated conductor includes a conductor and a coating on the conductor, the coating including the polymeric composition. The polymeric composition is at least partially disposed around the conductor to produce the coated conductor.
The process for producing a coated conductor includes mixing and heating the polymeric composition to at least the melting temperature of the silane functionalized polyolefin in an extruder, and then coating the polymeric melt blend onto the conductor. The term “onto” includes direct contact or indirect contact between the polymeric melt blend and the conductor. The polymeric melt blend is in an extrudable state.
The polymeric composition is disposed around on and/or around the conductor to form a coating. The coating may be one or more inner layers such as an insulating layer. The coating may wholly or partially cover or otherwise surround or encase the conductor. The coating may be the sole component surrounding the conductor. Alternatively, the coating may be one layer of a multilayer jacket or sheath encasing the metal conductor. The coating may directly contact the conductor. The coating may directly contact an insulation layer surrounding the conductor.
The resulting coated conductor (cable) is cured at humid conditions for a sufficient length of time such that the coating reaches a desired degree of crosslinking. The temperature during cure is generally above 0° C. In an embodiment, the cable is cured (aged) for at least 4 hours in a 90° C. water bath. In an embodiment, the cable is cured (aged) for up to 30 days at ambient conditions comprising an air atmosphere, ambient temperature (e.g., 20° C. to 40° C.), and ambient relative humidity (e.g., 10 to 96 percent relative humidity (% RH)).
The coated conductor may pass the horizontal burn test. To pass the horizontal burn test, the coated conductor must have a total char of less than 100 mm and the cotton placed underneath must not ignite. A time to self-extinguish of less than 80 seconds is desirable. The coated conductor may have a total char during the horizontal burn test from 0 mm, or 5 mm, or 10 mm to 50 mm, or 55 mm, or 60 mm, or 70 mm, or 75 mm, or 80 mm, or 90 mm, or less than 100 mm. The coated conductor may have a time to self-extinguish during the horizontal burn test from 0 seconds, or 5 seconds, or 10 seconds to 30 seconds, or 35 seconds, or 40 seconds, or 50 seconds, or 60 seconds, or 70 seconds, or less than 80 seconds.
The coated conductor may pass the VW-1 test. To pass the VW-1 test and thus have a VW-1 rating, the coated conductor must self-extinguish within 60 seconds (<60 seconds) of the removal of a burner for each of five 15 second flame impingement cycles, exhibit less than or equal to 25% flag burn, and exhibit no cotton burn. The VW-1 test is more stringent than the horizontal burn test. In an embodiment, the coated conductor has a time to self-extinguish during the VW-1 test from 0 seconds to 20 seconds, or 30 seconds, or 40 seconds, or 50 seconds, or 60 seconds, or less than 60 seconds during each of the 5 individual cycles. In an embodiment, the coated conductor has a no char to flag length during the VW-1 test from 20 mm, or 40 mm, or 50 mm, or 75 mm to 100 mm, or 110 mm, or 120 mm, or 130 mm, or 140 mm, or 150 mm, or 160 mm, or 180 mm, or 200 mm, or 250 mm.
The coated conductor has one, some, or all of the following properties: (i) a total char during the horizontal burn test from 0 mm to less than 100 mm; (ii) a time to self-extinguish during the horizontal burn test from 0 seconds to less than 80 seconds; (iii) a time to self-extinguish during the VW-1 test from 0 seconds to less than 60 seconds during each of the 5 individual cycles. The coated conductor may pass the Horizontal Burn Test and/or the VW-1 Burn Test.
Density: Density is measured in accordance with ASTM D792, Method B. The result is recorded in grams (g) per cubic centimeter (g/cc).
Melt Index: Melt index (MI) is measured in accordance with ASTM D1238, Condition 190° C./2.16 kilogram (kg) weight and is reported in grams eluted per 10 minutes (g/10 min).
Thermogravimetric Analysis: Thermogravimetric Analysis testing is performed using a Q5000 thermogravimetric analyzer from TA INSTRUMENTS™. Perform Thermogravimetric Analysis testing by placing a sample of the material in the thermogravimetric analyzer on platinum pans under nitrogen at flow rate of 100 cm3/minute and, after equilibrating at 40° C., raising the temperature from 40° C. to 650° C. at a rate of 20° C./minute while measuring the mass of the sample. From the curve of data generated associating a temperature with a % of mass remaining, determine the temperature at which 5% of the mass of the sample was lost to get the Temperature of 5% Mass Loss. From the curve of data generated associating a temperature with a % of mass remaining, determine the mass % of the sample remaining when the Thermogravimetric Analysis reaches 650° C. to get the Retained Mass at 650° C.
Crystallinity Testing: determine melting peaks and percent (%) or weight percent (wt %) crystallinity of ethylene-based polymers at 23° C. using Differential Scanning calorimeter (DSC) instrument DSC Q1000 (TA Instruments). (A) Baseline calibrate DSC instrument. Use software calibration wizard. Obtain a baseline by heating a cell from −80° to 280° C. without any sample in an aluminum DSC pan. Then use sapphire standards as instructed by the calibration wizard. Analyze 1 to 2 milligrams (mg) of a fresh indium sample by heating the standards sample to 180° C., cooling to 120° C. at a cooling rate of 10° C./minute, then keeping the standards sample isothermally at 120° C. for 1 minute, followed by heating the standards sample from 120° C. to 180° C. at a heating rate of 10° C./minute. Determine that indium standards sample has heat of fusion=28.71±0.50 Joules per gram (J/g) and onset of melting=156.6°±0.5° C. (B) Perform DSC measurements on test samples using the baseline calibrated DSC instrument. Press test sample of semi-crystalline ethylenic polymer into a thin film at a temperature of 160° C. Weigh 5 to 8 mg of test sample film in aluminum DSC pan. Crimp lid on pan to seal pan and ensure closed atmosphere. Place lid-sealed pan in DSC cell, equilibrate cell at 30° C., and then heat at a rate of about 100° C./minute to 190° C., keep sample at 190° C. for 3 minutes, cool sample at a rate of 10° C./minute to −60° C. to obtain a cool curve heat of fusion (Hf), and keep isothermally at −60° C. for 3 minutes. Then heat sample again at a rate of 10° C./minute to 190° C. to obtain a second heating curve heat of fusion (ΔHf). Using the second heating curve, calculate the “total” heat of fusion (J/g) by integrating from −20° C. (in the case of ethylene homopolymers, copolymers of ethylene and hydrolysable silane monomers, and ethylene alpha olefin copolymers of density greater than or equal to 0.90 g/cm3) or −40° C. (in the case of copolymers of ethylene and unsaturated esters, and ethylene alpha olefin copolymers of density less than 0.90 g/cm3) to end of melting. Using the second heating curve, calculate the “room temperature” heat of fusion (J/g) from 23° C. (room temperature) to end of melting by dropping perpendicular at 23° C. Measure and report “total crystallinity” (computed from “total” heat of fusion) as well as “Crystallinity at room temperature” (computed from 23° C. heat of fusion). Crystallinity is measured and reported as percent (%) or weight percent (wt %) crystallinity of the polymer from the test sample's second heating curve heat of fusion (ΔHf) and its normalization to the heat of fusion of 100% crystalline polyethylene, where % crystallinity or wt % crystallinity=(ΔHf*100%)/292 J/g, wherein ΔHf is as defined above, * indicates mathematical multiplication, / indicates mathematical division, and 292 J/g is a literature value of heat of fusion (ΔHf) for a 100% crystalline polyethylene.
VW-1 Burn Test: The VW-1 Burn Test is conducted by subjecting three or six samples of a specific coated conductor to the protocol of UL 2556 Section 9.4. This involves five 15-second applications of a 125 mm flame impinging on at an angle 20° on a vertically oriented specimen 610 mm (24 in) in length. A strip of kraft paper 12.5±1 mm (0.5±0.1 in) is affixed to the specimen 254±2 mm (10±0.1 in) above the impingement point of the flame. A continuous horizontal layer of cotton is placed on the floor of the test chamber, centered on the vertical axis of the test specimen, with the upper surface of the cotton being 235±6 mm (9.25±0.25 in) below the point at which the tip of the blue inner cone of the flame impinges on the specimen. Test failure is based upon the criteria of either burning the 25% of the kraft paper tape flag, ignition of the cotton batting or if the specimen burns longer than 60 seconds on any of the five flame applications. As an additional measure of burn performance, the length of uncharred insulation (“no char to flag length”) is measured at the completion of the test. The VW-1 cotton ignited indicates if falling material ignited the cotton bed.
Horizontal Burn Test: The Horizontal Burn Test is conducted in accordance with UL-2556. The test is performed by placing the coated conductor in a horizontal position. Cotton is placed underneath the coated conductor. A burner is set at a 20° angle relative to the horizontal sample (14 AWG copper wire with 30 mil coating wall thickness). A one-time flame is applied to the middle of the sample for 30 seconds. The sample fails when (i) the cotton ignites and/or (ii) the sample chars in excess of 100 mm Char length is measured in accordance with UL-1581, 1100.4. The test is repeated 3 times.
Molecular Weight: Unless otherwise denoted herein, molecular weight is the weight average molecular weight and is determined by gel permeation chromatography. Gel permeation chromatography (GPC) is performed on a Waters 150° C. high temperature chromatographic unit equipped with three linear mixed bed columns (Polymer Laboratories (10 micron particle size)), operating at a system temperature of 140° C. The solvent is 1,2,4-trichlorobenzene from which about 0.5% by weight solutions of the samples are prepared for injection. The flow rate is 1.0 milliliter/minute (mm/min) and the injection size is 100 microliters (:l). The molecular weight determination is deduced by using narrow molecular weight distribution polystyrene standards (from Polymer Laboratories) in conjunction with their elution volumes. The equivalent polyethylene molecular weights are determined by using appropriate Mark-Houwink coefficients for polyethylene and polystyrene (as described by Williams and Ward in Journal of Polymer Science, Polymer Letters, Vol. 6, (621) 1968) to derive the equation:
M
polyethylene=(a)(Mpolystyrene)b
In this equation, a=0.4316 and b=1.0. Weight average molecular weight (Mw) is calculated in the usual manner according to the formula:
M
w=Σ(wi)(Mi)
in which wi and Mi are the weight fraction and molecular weight respectively of the ith fraction eluting from the GPC column.
Differential Scanning calorimetry (DSC): DSC is used to measure the melting, crystallization, and glass transition behavior of a polymer over a wide range of temperature. DSC is performed using a TA Instruments Q1000 DSC equipped with refrigerated cooling system and an autosampler. During testing, a nitrogen purge gas flow of 50 ml/min is used. Each sample is melt pressed into a thin film at 190° C.; the melted sample is then air-cooled to 25° C. (i.e., ambient conditions). A 3 mg to 10 mg, 6 mm diameter specimen is extracted from the cooled polymer, weighed, placed in a light aluminum pan (50 mg), and crimped shut. Analysis is then performed to determine its thermal properties. The thermal behavior of the sample is determined by ramping the sample temperature up and down to create a heat flow versus temperature profile. First, the sample is rapidly heated to 180° C. and held isothermal for 3 minutes in order to remove its thermal history. Next, the sample is cooled to −80° C. at a 10° C./minute cooling rate and held isothermal at −80° C. for 3 minutes. The sample is then heated to 180° C. (this is the “second heat” ramp) at a 10° C./minute heating rate. The cooling and second heating curves are recorded. The values determined are the extrapolated onset of melting, Tm, and the extrapolated onset of crystallization, Tc. Melting point, Tm, is determined from the DSC heating curve by first drawing the baseline between the start and end of the melting transition. A tangent line is then drawn to the data on the low temperature side of the melting peak. Where this line intersects the baseline is the extrapolated onset of melting (Tm). This is as described in Bernhard Wunderlich, The Basis of Thermal Analysis, in Thermal Characterization of Polymeric Materials 92, 277-278 (Edith A. Turi ed., 2d ed. 1997). Crystallization temperature, Tc, is determined from a DSC cooling curve as above except the tangent line is drawn on the high temperature side of the crystallization peak. Where this tangent intersects the baseline is the extrapolated onset of crystallization (Tc).
The materials used in the examples are provided below.
SiPO is an ethylene/silane copolymer having a density of 0.922 g/cc, a crystallinity at 23° C. of 46.9 wt % and a melt index of 1.5 g/10 min (190° C./2.16 kg) and is commercially available as SI-LINK™ DFDA-5451 NT from The Dow Chemical Company, Midland, Mich.
LLDPE is a linear low-density polyethylene resin having a density of 0.920 g/cc, a crystallinity at 23° C. of 49 wt % and a melt index of 3.5 g/10 min (190° C./2.16 kg) and is commercially available as DOW™ LLDPE 1648 from The Dow Chemical Company, Midland, Mich.
BRFR 3010 is an aromatically brominated polystyrene having a bromine content of 68.5 wt %, a weight average molecular weight of 4,700 g/mol as measured using gel permeation chromatography, a Temperature of 5% Mass Loss of 373° C. as measured according to Thermogravimetric Analysis, a Retained Mass at 650° C. of 1.5 mass % as measured according to Thermogravimetric Analysis, and a glass transition temperature of 163° C. as measured by Differential Scanning calorimetry and is commercially available under the tradename Saytex™ HP-3010 from Albemarle, Charlotte, N.C., United States.
AT is Sb2O3 commercially available as BRIGHTSUN™ HB500 from China Antimony Chemicals Co. Ltd, Beijing, China.
ZnFR is zinc oxide commercially available as grade 104 from Zochem LLC, Dickson, Tenn.
AO1 is a sterically hindered phenolic antioxidant having the chemical name pentaerythritol tetrakis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate), which is commercially available as IRGANOX™ 1010 from BASF, Ludwigshafen, Germany.
AO2 is a phenolic antioxidant (CAS 32687-78-8); density=1.11 g/cc., 2′,3-bis[[3-[3,5-di-tert-butyl-4-hydroxyphenyl]propionyl]]propionohydrazide, and is commercially available as IRGANOX™ 1024 from BASF, Ludwigshafen, Germany.
CM2 is a catalyst masterbatch blend of polyolefins, phenolic compounds, and 2.6 wt % of dibutyltin dilaurate as silanol condensation catalyst.
Catalyst is a dibutyltin dilaurate catalyst having a CAS number of 77-58-7 and commercially available under the tradename FASCAT™ 4202 PMC Organometallix, Mount Laurel, N.J., US.
CM3 is a hindered amine light stabilizer masterbatch containing 97 wt % of an ethylene-ethyl acrylate Copolymer (15 wt % ethyl acrylate) having a density of 0.930 g/cc, a crystallinity at 23° C. of 33 wt % and a melt index of 1.3 g/10 min (190° C./2.16 kg) and 3 wt % of CHIMASSORB™ 119, a hindered amine light stabilizer available from BASF.
Inventive Examples (“IE”) 1-IE3 were prepared by preheating a BRABENDER™ mixer to 190° C. Once preheated, the entire BRFR 3010 used in IE-IE3 was added to the mixer and blended for 3 minutes at 30 revolutions per minute (“rpm”) to ensure that the BRFR 3010 was at least 5° C. or greater above its glass transition temperature (163° C.). Next the LLDPE was added to the mixer and allowed to soften and homogenize with the BRFR 3010 during mixing for an additional 3 minutes at 30 RPM. The remainder of the materials of IE1-IE3 except the SI-LINK™ AC DFDB-5451 NT were added to the combined BRFR and LLDPE and mixed for 5 minutes at 50 RPM at 190° C.
Comparative Example (“CE”) 1 was performed by combining all the ingredients of Table 1 except the SI-LINK™ AC DFDB-5451 NT together and melt blending the mix at 50 rpm, at 190° C. for 10 minutes using a BRABENDER™ mixer with Cam blades.
The melt blended materials of IE1-IE3 and CE1 were removed from the mixer and cold-pressed for 3 minutes with room-temperature platens at 2500 psi, and were then guillotined into strips. The strips were pelletized in preparation for extrusion. The pellets were then dried in a vacuum oven for 16 hours at 60° C. at a pressure of 6772.78 pascals. The pellets were first dry blended with the SI-LINK™ AC DI-DB-5451 NT and then melt blended using a ¾ inch BRABENDER™ extruder and a standard polyethylene screw equipped with a pineapple mixing section. The IE and CE were extruded onto a 14 American wire gauge solid copper wire to form cables having polymeric sheaths of 0.762 millimeter thickness. The set temperature profile on the extruder was 160/170/180/190° C., with measured melt temperatures ranging from 185° C. to 195° C. The cables were cured in a 90° C. water bath for 16 hours after which the VW-1 Burn Test was performed.
Table 1 provide compositional and burn performance data on IE1-IE3 and CE1.
As evident from Table 1, IE1-IE3 and CE1 all have substantially similar compositions, but have different outcomes when subjected to the VW-1 Burn Test. As can be seen, IE1-IE3 pass the VW-1 Burn Test while CE1 does not. Without being bound by theory, it is believed that by following the multistep melt blending process of heating the PBFR to a temperature of 5° C. or greater above its glass transition temperature, then mixing the LLDPE into the PBFR followed by adding the inorganic fillers allows for a substantially more homogenous mixture to form. Despite the similar composition, CE1 fails the VW-1 Burn Test due to an incomplete mixing as a result of its single-step melt blending. As can be seen, despite having nearly identical bromine concentrations IE3 is able to pass the VW-1 Burn Test while CE1 is not. It is believed that the single-step melt blending leads to agglomerations of the PBFR and the fillers which in turn creates discrete domains of unprotected polyolefin, leading to increased flammability. As a result, the multistep melt blending of IE1-IE3 provides surprising flame retardancy benefits to a substantially similar composition over the single step melt blending of CE1. Although not tested, it is believed that IE1-IE3 would pass the Horizontal Burn Test because each of these examples passed the more rigorous VW-1 Burn Test.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/US2021/040151 | 7/1/2021 | WO |
| Number | Date | Country | |
|---|---|---|---|
| 63051027 | Jul 2020 | US |
