Flame-retardant, cross-linked EPDM rubber
09879121 ยท 2018-01-30
Assignee
Inventors
- Sarah K. Czaplewski (Rochester, MN, US)
- Joseph Kuczynski (North Port, FL)
- Jason T. Wertz (Pleasant Valley, NY)
- Jing Zhang (Poughkeepsie, NY, US)
Cpc classification
C08F210/18
CHEMISTRY; METALLURGY
C08L23/16
CHEMISTRY; METALLURGY
C08G2261/1426
CHEMISTRY; METALLURGY
C08G2261/418
CHEMISTRY; METALLURGY
C08F4/6592
CHEMISTRY; METALLURGY
C08J2319/00
CHEMISTRY; METALLURGY
C08G2261/147
CHEMISTRY; METALLURGY
C08F4/65908
CHEMISTRY; METALLURGY
C08J2323/16
CHEMISTRY; METALLURGY
C08G61/08
CHEMISTRY; METALLURGY
C08J3/24
CHEMISTRY; METALLURGY
C08F210/18
CHEMISTRY; METALLURGY
C08C19/24
CHEMISTRY; METALLURGY
C08F8/40
CHEMISTRY; METALLURGY
C08F4/6592
CHEMISTRY; METALLURGY
C08C19/28
CHEMISTRY; METALLURGY
International classification
C08J3/24
CHEMISTRY; METALLURGY
C08C19/24
CHEMISTRY; METALLURGY
C08F210/18
CHEMISTRY; METALLURGY
Abstract
In an example, a process includes polymerizing a mixture that includes an ethylene monomer, a propylene monomer, and a diene monomer to form an ethylene-propylene-diene (EPDM) terpolymer using ring-opening metathesis polymerization (ROMP). The process further includes chemically reacting the EPDM terpolymer with a norbornene-based phosphinate cross-linking material to form a flame-retardant, cross-linked EPDM rubber.
Claims
1. A process comprising: polymerizing a mixture that includes an ethylene monomer, a propylene monomer, and a diene monomer to form an ethylene-propylene-diene (EPDM) terpolymer and chemically reacting the EPDM terpolymer with a norbornene-based phosphinate cross-linking material by a ring-opening reaction to form a flame-retardant, cross-linked EPDM rubber.
2. The process of claim 1, wherein the ethylene monomer includes chlorinated ethylene.
3. The process of claim 1, wherein the diene monomer includes 5-ethylidene -2- norbornene, 5-propylidene-2-norbornene, or a combination thereof.
4. The process of claim 1, wherein forming the EPDM terpolymer includes using a mixture of Cp*TiMe.sub.3 and B(C.sub.6F.sub.5).sub.3 as a catalyst material.
5. The process of claim 4, wherein at least a portion of the catalyst material remains after formation of the flame-retardant, cross-linked EPDM rubber.
6. The process of claim 1, further comprising chemically reacting a norbornene-based alcohol and a phosphinate material to form the norbornene-based phosphinate cross-linking material.
7. The process of claim 6, wherein the norbornene-based alcohol includes 5-norbornene-2-methanol.
8. The process of claim 6, wherein the phosphinate material includes 3- (hydroxyl(phenyl)phosphoryl)propanoic acid.
9. A process comprising: polymerizing a mixture that includes a chlorinated ethylene monomer, a propylene monomer, and a diene monomer to form a chlorinated ethylene-propylene-diene (EPDM) terpolymer; chemically reacting a norbornene-based alcohol and a phosphinate material to form a norbornene-based phosphinate cross-linking material; and chemically reacting the chlorinated EPDM terpolymer with the norbornene-based phosphinate cross-linking material by a ring-opening reaction to form a flame-retardant, cross-linked chlorinated EPDM rubber.
10. The process of claim 9, wherein a weight percentage of the chlorinated ethylene monomer is in a range of 30 to 80 weight percent of the mixture.
11. The process of claim 9, wherein a weight percentage of the diene monomer is in a range of 2 to 10 weight percent of the mixture.
12. The process of claim 9, wherein the norbornene-based alcohol includes 5- norbornene-2-methanol.
13. The process of claim 9, wherein the phosphinate material includes 3- (hydroxyl(phenyl)phosphoryl)propanoic acid.
14. An article of manufacture comprising: a flame-retardant, cross-linked ethylene-propylene-diene (EPDM) rubber that is cross-linked using a norbornene-based phosphinate cross-linking material.
15. The article of manufacture of claim 14, further comprising Cp*TiMe.sub.3 and B(C.sub.6F.sub.5).sub.3.
16. The article of manufacture of claim 14, wherein chlorine (Cl) is incorporated into a polymer backbone of the flame-retardant, cross-linked EPDM rubber.
Description
IV. BRIEF DESCRIPTION OF THE DRAWINGS
(1)
(2)
(3)
V. DETAILED DESCRIPTION
(4) The present disclosure relates to flame-retardant, cross-linked EPDM rubber materials and methods of preparing flame-retardant, cross-linked EPDM rubber materials. In the present disclosure, ring-opening metathesis polymerization may be used to polymerize a mixture of an ethylene monomer (e.g., chlorinated ethylene, in some cases), a propylene monomer, and a diene monomer to form an EPDM terpolymer. The EPDM terpolymer may be chemically reacted with a norbornene-based phosphinate cross-linking material to form a flame-retardant, cross-linked EPDM rubber. Utilization of a norbornene-based phosphinate material as a cross-linking agent may allow for incorporation of a flame retardant agent (phosphorus) directly into a backbone of an EPDM rubber material. Further, in cases where a chlorinated ethylene monomer is used to form the EPDM terpolymer, the incorporation of chlorine into the EPDM terpolymer chains may provide additional flame retardancy benefits.
(5) Referring to
(6) Referring to the chemical reaction depicted at the bottom of
(7) In a particular embodiment, a weight percentage of the ethylene monomer (chlorinated ethylene, in this case) may be in a range of 30 to 80 weight percent of the mixture. In a particular embodiment, a weight percentage of the diene monomer may be in a range of 2 to 10 weight percent of the mixture. A weight percentage of the propylene monomer may be in a range of 10 weight percent to 68 weight percent, depending on the relative weight percentages of the ethylene/diene monomers in the mixture. It will be appreciated that the weight percentages of the monomers may be selected in order to form an EPDM terpolymer with a first portion (illustrated by the integer m) corresponding to the chlorinated ethylene monomer, a second portion (illustrated by the integer n) corresponding to the propylene monomer, and a third portion (illustrated by the integer o) corresponding to the diene monomer.
(8)
PROPHETIC EXAMPLE
Preparation of a Chlorinated EPDM Terpolymer
(9) To a cooled (8 C.) glass reactor containing a solution of Cp.TiMe.sub.3 (14 mg, 0.06 mmol) in 5 mL of toluene, a cooled (8 C.) solution of B(C.sub.6F.sub.5).sub.3 (31 mg, 0.06 mmol) in 5 mL of toluene may be added. The mixture may be bubbled for about 10 minutes through a mixture of vinyl chloride and propylene (e.g., in about a 1:1 ratio). To the EPDM polymerization reaction, diene monomer such as ENB (e.g., about 2-10 wt %) may be added prior to the addition of B(C.sub.6F.sub.5).sub.3. Bubbling of the vinyl chloride/propylene mixture through the stirred, cooled solution may be continued for about 5-10 minutes. After reaction time, the viscous mixture may be treated with methanol (5 mL). The reaction temperature during polymerization may increase to about 18 C. and may remain constant until termination of the reaction. The resultant chlorinated EPDM terpolymer may then be purified. In some cases, trace amounts of catalyst material (e.g., Cp.TiMe.sub.3 and/or B(C.sub.6F.sub.5).sub.3) may remain after purification.
(10) Referring to the chemical reaction diagram depicted at the top of
PROPHETIC EXAMPLE
Preparation of Norbornene-Based Phosphinate Cross-Linking Material
(11) To a 250 mL round bottom flask fitted with a condenser, 5-Norbornene-2-methanol (100 mL) may be added followed by 3-(hydroxyl(phenyl)phosphoryl)propanoic acid (149 mmol) to form a mixture. The mixture may then be stirred under ambient temperature. Sulfuric acid (3.66 g; 37.3 mmol) may be added, followed by heating the reaction to about 65 C. and holding for about 3 hours. After reaction, the solution may be cooled below room temperature for about 6 hours to allow precipitation. The product may then be purified.
(12) Referring to the chemical reaction illustrated in the middle of
(13) In a particular embodiment, an amount of norbornene-based phosphinate cross-linking material that is chemically reacted with the chlorinated EPDM terpolymer may be sufficient for the flame-retardant, cross-linked chlorinated EPDM rubber to satisfy one or more plastics flammability standards. In some cases, additional flame retardant packages may be added in order to satisfy plastics flammability standard(s). To illustrate, a plastics flammability standard may be associated with heat-shrink tubing. As an example, the plastics flammability standard (e.g., associated with heat-shrink tubing) may include a burning stop rate of not greater than 60 seconds on a vertical specimen of an article of manufacture that includes the flame-retardant, cross-linked chlorinated EPDM rubber (e.g., EPDM rubber tubing for a water cooling application). In some cases, the plastics flammability standard may allow drips of non-inflamed particles but may not allow drips of flaming particles.
PROPHETIC EXAMPLE
Cross-Linking of Chlorinated EPDM Terpolymer
(14) To an internal mixer, chlorinated EPDM (94.3 wt %), elemental sulfur (0.7 wt %), an accelerator (such as MBT; 1 wt %), zinc oxide (3 wt %), and steric acid (1 wt %) may be added. Accelerators and activators and vulcanizing routes (e.g., sulfur, peroxide, etc.) may be selected by one of ordinary skill in the art. To the reaction, (3-((bicycle[2.2.1]hept-5-en-2-ylmethyl)peroxy)propyl)(phenyl)phosphinic acid (e.g., 1 equiv.) may be added. The mixture may then be heated in an internal mixture to about 130-140 C. The rubber may be cured at about 160-180 C.
(15) Thus,
(16) Referring to
(17) Referring to the chemical reaction depicted at the bottom of
(18) It will be appreciated that the weight percentages of the monomers may be selected in order to form an EPDM terpolymer with a first portion (illustrated by the integer w) corresponding to the ethylene monomer, a second portion (illustrated by the integer x) corresponding to the propylene monomer, and a third portion (illustrated by the integer y) corresponding to the diene monomer. As the embodiment illustrated in
(19)
PROPHETIC EXAMPLE
Preparation of EPDM Terpolymer
(20) To a cooled (8 C.) glass reactor containing a solution of Cp.TiMe.sub.3 (14 mg, 0.06 mmol) in 5 mL of toluene, a cooled (8 C.) solution of B(C.sub.6F.sub.5).sub.3 (31 mg, 0.06 mmol) in 5 mL of toluene may be added. The mixture may be bubbled for about 10 minutes through a mixture of ethylene and propylene (e.g., in about a 1:1 ratio). To the EPDM polymerization reaction, diene monomer such as ENB may be added prior to the addition of B(C.sub.6F.sub.5).sub.3. Bubbling of the ethylene/propylene mixture through the stirred, cooled solution may be continued for about 5-10 minutes. After reaction time, the viscous mixture may be treated with methanol (5 mL). The reaction temperature during polymerization may increase to about 18 C. and may remain constant until termination of the reaction. The resultant EPDM terpolymer may then be purified. In some cases, trace amounts of catalyst material (e.g., Cp.TiMe.sub.3 and/or B(C.sub.6F.sub.5).sub.3 may remain after purification.
(21) Referring to the chemical reaction illustrated at the top of
(22) In a particular embodiment, an amount of norbornene-based phosphinate cross-linking material that is chemically reacted with the EPDM terpolymer may be sufficient for the flame-retardant, cross-linked EPDM rubber to satisfy one or more plastics flammability standards. In some cases, additional flame retardant packages may be added in order to satisfy plastics flammability standard(s), such as a plastics flammability standard associated with heat-shrink tubing. As an example, a plastics flammability standard may include a burning stop rate of not greater than 60 seconds on a vertical specimen of an article of manufacture that includes the flame-retardant, cross-linked EPDM rubber (e.g., EPDM rubber tubing for a water cooling application). In some cases, the plastics flammability standard may allow drips of non-inflamed particles but may not allow drips of flaming particles.
PROPHETIC EXAMPLE
Cross-Linking of EPDM Terpolymer
(23) To an internal mixer, EPDM (94.3 wt %), elemental sulfur (0.7 wt %), an accelerator (such as MBT; 1 wt %), zinc oxide (3 wt %), and steric acid (1 wt %) may be added. Accelerators and activators and vulcanizing routes (e.g., sulfur, peroxide, etc.) may be selected by one of ordinary skill in the art. To the reaction, (3-((bicycle[2.2.1]hept-5-en-2-ylmethyl)peroxy)propyl)(phenyl)phosphinic acid (1 equiv.) may be added. The mixture may then be heated in an internal mixture to about 130-140 C. The rubber may be cured at about 160-180 C.
(24) Thus,
(25)
(26) The process 300 includes forming an EPDM terpolymer by ring-opening metathesis polymerization, at 302. As an example, referring to
(27) The process 300 includes chemically reacting the EPDM terpolymer with a norbornene-based phosphinate cross-linking material to form a flame-retardant, cross-linked EPDM rubber, at 304. As an example, referring to
(28) In the particular embodiment illustrated in
(29) Thus,
(30) The previous description of the disclosed embodiments is provided to enable any person skilled in the art to make or use the disclosed embodiments. Various modifications to these embodiments will be readily apparent to those skilled in the art, and the generic principles defined herein may be applied to other embodiments without departing from the scope of the disclosure. Thus, the present disclosure is not intended to be limited to the embodiments shown herein but is to be accorded the widest scope possible consistent with the principles and features as defined by the following claims.