Patent Application
20200308403
This disclosure relates to compositions that cure to form polythioether polymers and that include a dual cure curing mechanism, as well as sealants comprising the same.
Briefly, the present disclosure provides compositions that are curable to polythioether polymers, comprising: a) a dithiol monomer; b) a diene monomer; c) a radical cleaved photoinitiator; d) a peroxide; and e) an amine; where the peroxide and amine together are a peroxide-amine redox initiator. In some embodiments, the amine is a tertiary amine. In some embodiments, the amine is selected from the group consisting of dihydroxyethyl-p-toluidine, N,N-diisopropylethylamine, and N, N, N′, N″, N″-pentamethyl-diethylenetriamine. In some embodiments, the peroxide is selected from the group consisting of di-tert-butyl peroxide, methyl ethyl ketone peroxide, and benzoyl peroxide. In some embodiments, the composition may additionally comprise a polythiol monomer having three or more thiol groups. In some embodiments, the composition may additionally comprise one or more fillers. In some embodiments, the composition may additionally comprise one or more nanoparticle fillers. In some embodiments, the composition may additionally comprise calcium carbonate. In some embodiments, the composition may additionally comprise nanoparticle calcium carbonate. In some embodiments, the composition may be cured by application of light from an actinic light source. In some embodiments, the composition may be cured by application of light from a blue light source. In some embodiments, the composition may be cured by application of light from a UV light source.
In another aspect, the present disclosure provides sealants comprising curable compositions according to the present disclosure. In another aspect, the present disclosure provides seals obtained by cure of such sealants.
In another aspect, the present disclosure provides polythioether polymers obtained by cure of any the compositions according to the present disclosure. In some embodiments, the polythioether polymer has a Tg less than −50° C. In some embodiments, the polythioether polymer exhibits high jet fuel resistance characterized by a volume swell of less than 30% and a weight gain of less than 20% when measured according to Society of Automotive Engineers (SAE) International Standard AS5127/1.
All scientific and technical terms used herein have meanings commonly used in the art unless otherwise specified.
As used in this specification and the appended claims, the singular forms “a”, “an”, and “the” encompass embodiments having plural referents, unless the content clearly dictates otherwise.
As used in this specification and the appended claims, the term “or” is generally employed in its sense including “and/or” unless the content clearly dictates otherwise.
As used herein, “have”, “having”, “include”, “including”, “comprise”, “comprising” or the like are used in their open ended sense, and generally mean “including, but not limited to.” It will be understood that the terms “consisting of” and “consisting essentially of” are subsumed in the term “comprising,” and the like.
The present disclosure provides a dual cure polythioether material such as a sealant. In some embodiments the sealant has both cure on demand properties and dark cure properties. In some embodiments the sealant may be cured by exposure to actinic radiation in 120 seconds or less, in some embodiments 90 seconds or less, in some embodiments 60 seconds or less, in some embodiments 30 seconds or less, and in some embodiments 20 seconds or less. In some embodiments cure on demand can be initiated with UV light, in some with visible light, in some with LED sourced UV light, and in some with LED sourced visible light. Furthermore, in some embodiments the initially photoinitiated cure propagates by a dark cure mechanism into adjacent portions of the polythioether material that are without light access. In some embodiments cure propagates by at least 2.5 cm into the dark zone with 90% or greater conversion in 120 seconds or less, in some embodiments 90 seconds or less, in some embodiments 60 seconds or less, in some embodiments 30 seconds or less, and in some embodiments 20 seconds or less. In some embodiments cure propagates by at least 5.0 cm into the dark zone with 90% or greater conversion in 120 seconds or less, in some embodiments 90 seconds or less, in some embodiments 60 seconds or less, in some embodiments 30 seconds or less, and in some embodiments 20 seconds or less.
With reference to
In some embodiments, the initiation system includes a) a radical cleaved photoinitiator and b) a peroxide-amine redox initiator.
In some embodiments, the cured material has low glass transition temperature, in some embodiments less than −20° C., in some embodiments less than −30° C., in some embodiments less than −40° C., and in some embodiments less than −50° C. In some embodiments, the cured material has excellent fuel resistance properties. In some embodiments, the cured material combines low glass transition temperature of less than −50° C. with excellent fuel resistance properties. Thus, in certain embodiments this dual cure technology can be applied to aircraft or automobile sealant applications and may result in greater ease and speed of vehicle manufacture.
The following numbered embodiments are intended to further illustrate the present disclosure but should not be construed to unduly limit this disclosure.
a) a dithiol monomer;
b) a diene monomer;
c) a radical cleaved photoinitiator;
d) a peroxide; and
e) an amine;
f) a polythiol monomer having three or more thiol groups.
g) at least one filler.
h) at least one nanoparticle filler.
j) calcium carbonate.
k) nanoparticle calcium carbonate.
Objects and advantages of this disclosure 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 disclosure.
Unless otherwise noted, all reagents were obtained or are available from Sigma-Aldrich Company, St. Louis, Mo., or may be synthesized by known methods. Unless otherwise reported, all ratios are by weight percent.
° C.: degrees Centigrade
cm: centimeter
LED: light emitting diode
mL: milliliter
Mn: Molecular weight
mW: milliWatt
nm: nanometer
Tg: glass transition temperature
UV: ultraviolet
PTE-1. Into a 1000-mL round bottom flask equipped with an air-driven stirrer, thermometer, and a dropping funnel, was added 392.14 grams (2.15 moles) DMDO and 82.23 grams (0.25 moles) E-8220. To this mixture was added 0.15 grams DABCO. The system was flushed with nitrogen, then mixed and heated for four hours at 60-70° C. 12.5 grams (0.05 moles) TAC was added, followed by approximately 0.15 grams VAZO 67.
With continuous stirring, the mixture was heated to 60° C., and held at this temperature for approximately 30-45 minutes. 313.13 grams (1.55 moles) DVE-3 were slowly added drop-wise to the flask over a period of 45-60 minutes, keeping the temperature at approximately between 68-80° C. Additional VAZO 67 was added in approximately 0.15 gram increments over approximately 6 hours, for a total of approximately 0.6 grams. The temperature was raised to 100° C. and the material degassed for approximately 10 minutes. The resultant polythioether was approximately 3200 Mn with a 2.2 functionality.
PTE-2. Into a 500 mL four-neck, round bottom flask fitted with a stirrer, thermometer, chilled water condenser and a pressure equalizing addition funnel was added 206.54 grams of a 20% aqueous solution of sodium hydroxide (1.033 moles). To this was added, drop wise with stirring, 94.08 grams (0.51 moles) DMDO, and the mixture then allowed to cool to approximately 21° C. 96.4 grams (1.065 moles) CMP was added drop wise with vigorous stirring, and stirring continued for another 2 hours. The mixture was then held at 21° C. for approximately 16 hours, after which 150 grams of a clear layer was decanted. NMR analysis confirmed the decanted layer to be CMP diene.
Into a 100-mL round bottom flask equipped with an air-driven stirrer, thermometer, and a dropping funnel, was added 39.64 grams (0.22 moles) DMDO and 4.10 grams (0.0125 moles) E-8220. To this mixture was added 0.02 grams DABCO. The system was flushed with nitrogen, then mixed and heated for 1.5 hours at 60-70° C. 3.66 grams (.0125 moles) CMP diene was added followed by approximately 0.01 grams VAZO 52. With continuous stirring, the mixture was heated to 60° C., and held at this temperature for approximately 1.5 hrs. 0.83 grams (0.005 mole) TVCH were added and the temperature maintained for another 1.5 hrs. 31.80 grams (0.157 moles) DVE-3 were slowly added drop-wise to the flask over a period of 45-60 minutes, keeping the temperature at approximately 70° C. Additional VAZO 52 was added in approximately 0.01 gram increments over approximately 16 hours, for a total amount of about 0.4 grams. The temperature is raised to 100° C. and the material degassed for approximately 10 minutes. The resultant polythioether was approximately 3200 Mn with a 2.2 functionality.
Part A was prepared by dissolving 0.0139 grams BPO and 0.0300 grams 1-819 in 3.0000 grams DVE-3 in a 20 mL amber vial, on a roll mill for 40 minutes at 21° C. Part B was prepared by dissolving 0.0139 grams DHEPT and 0.0394 grams 1-819 in 3.9407 grams TPTMP in a 20 mL amber vial, also on a roll mill for 8 hours at 21° C. Part A was then added to Part B and manually stirred for one minute until homogeneously dispersed.
The procedure generally described in Example 1 for preparing homogeneous mixtures of peroxide, photo initiator and vinyl monomer in Part A, and amine, photo initiator and thiol monomer in Part B, was repeated according to the formulations listed in Tables 1A and 1B.
Part A was prepared by dissolving 0.0347 grams BPO and 0.1549 grams 1-819 in 15.0000 grams DVE-3 in a 20 mL amber vial, on a roll mill for 40 minutes at 21° C. The solution was transferred to a speed mixer jar. 0.1000 grams A-200 and 5.3111 grams clay were added to the solution and homogeneously dispersed by means of a high speed mixer at 2,000 rpm for one minute. Part B was prepared by dissolving 0.0347 grams DIPEA and 0.1974 grams 1-819 in 19.7034 grams TPTMP in a 40 mL amber vial, also on a roll mill for 40 minutes at 21° C. The solution was transferred to a speed mixer jar. 0.1000 grams A-200 and 1.8916 grams clay were added to the solution and homogeneously dispersed by means of the high speed mixer at 2,000 rpm for one minute. Part A and Part B were homogeneously dispersed through a static mixer.
The procedure generally described in Example 9 for preparing homogeneous mixtures of Part A and Part B was repeated according to the formulations listed in Tables 1A and 1B.
The procedure generally described in Example 1 for preparing homogeneous mixtures of Part A and Part B was repeated according to the formulations listed in Tables 1A and 1B.
0.0694 grams 1-819 was dissolved in a mixture of in 3.0000 grams DVE-3 and 3.9407 grams TPTMP in a 20 mL amber vial, on a roll mill for 40 minutes at 21° C.
The procedure generally described in Example 1 for preparing homogeneous mixtures of Part A and Part B was repeated according to the formulations listed in Tables 1A and 1B.
0.0765 grams 1-819 was dissolved in a mixture of in 4.0000 grams DMDO and 3.3467 grams TAC in a 20 mL amber vial, on a roll mill for 40 minutes at 21° C.
The procedure generally described in Example 1 for preparing homogeneous mixtures of Part A and Part B was repeated according to the formulations listed in Tables 1A and 1B, wherein Part B was mixed for 24 hours rather than 8 hours.
The procedure generally described in Example 1 for preparing homogeneous mixtures of Part A and Part B was repeated according to the formulations listed in Tables 1A and 1B.
The following molds were used for curing evaluations:
Glass mold. An elongate 25 cm by 1.27 cm by 0.1 cm deep silicone rubber mold over a glass base, with an opaque silicone rubber sheet covering all but 1.27 cm of one end of the mold.
Aluminum, fit glass and black coated wood molds. An elongate 10 cm by 1.27 cm by 0.1 cm deep silicone rubber mold over an aluminum, fit glass or black coated wood base, with an opaque silicone rubber sheet covering all but 1.27 cm of one end of the mold.
Teflon™ mold. A 8.4 cm by 3.2 cm by 0.2 cm deep silicone rubber mold over a Teflon™ base, with an opaque silicone rubber sheet covering all but 2 cm of one end of the mold.
The curable composition was applied to the mold, an opaque silicone rubber sheet was then laid over the curable composition according to the dimensions described above. The remaining exposed area of the composition was then exposed to a 88 mW 455 nm LED light source, at a distance of 1.27 cm, for between 10-60 seconds. The following thiol-ene curing evaluations are listed in Tables 2 and 3.
The Tg of photo-initiated and redox-initiated Examples 1, 7, and 15 were measured using a model “DSC Q2000” differential scanning calorimeter, obtained from TA Instruments, New Castle, Del. Results are listed in Table 4.
Various modifications and alterations of this disclosure will become apparent to those skilled in the art without departing from the scope and principles of this disclosure, and it should be understood that this disclosure is not to be unduly limited to the illustrative embodiments set forth hereinabove.
This application is a continuation of U.S. application Ser. No. 15/533758 filed Jun. 7, 2017, now pending, which is a national stage filing under 35 U.S.C. 371 of PCT/US2015/067450, filed Dec. 22, 2015, which claims the benefit of Provisional Application No. 62/095952, filed Dec. 23, 2014, the disclosure of which is incorporated by reference in its/their entirety herein.
| Number | Date | Country | |
|---|---|---|---|
| 62095952 | Dec 2014 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 15533758 | Jun 2017 | US |
| Child | 16946253 | US |
