WO1999024491A1 - Chromate-free, one-part, non-curing corrosion inhibitive sealant with resistance to aviation fuel - Google Patents

Chromate-free, one-part, non-curing corrosion inhibitive sealant with resistance to aviation fuel Download PDF

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Publication number
WO1999024491A1
WO1999024491A1 PCT/US1998/023655 US9823655W WO9924491A1 WO 1999024491 A1 WO1999024491 A1 WO 1999024491A1 US 9823655 W US9823655 W US 9823655W WO 9924491 A1 WO9924491 A1 WO 9924491A1
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WO
WIPO (PCT)
Prior art keywords
composition
polysulfide
mixture
monoepoxy compound
sealant
Prior art date
Application number
PCT/US1998/023655
Other languages
French (fr)
Inventor
Alfredo Reyes, Jr.
Frank Campbell
Santo Randazzo
Original Assignee
Prc-Desoto International, Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Prc-Desoto International, Inc. filed Critical Prc-Desoto International, Inc.
Priority to JP2000520496A priority Critical patent/JP4157276B2/en
Priority to CA002309211A priority patent/CA2309211C/en
Priority to DE69806046T priority patent/DE69806046T2/en
Priority to EP98963753A priority patent/EP1032607B1/en
Priority to BR9813979-7A priority patent/BR9813979A/en
Priority to AU19011/99A priority patent/AU736628B2/en
Priority to KR1020007004841A priority patent/KR20010031775A/en
Publication of WO1999024491A1 publication Critical patent/WO1999024491A1/en

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K3/00—Materials not provided for elsewhere
    • C09K3/10—Materials in mouldable or extrudable form for sealing or packing joints or covers
    • C09K3/1006—Materials in mouldable or extrudable form for sealing or packing joints or covers characterised by the chemical nature of one of its constituents
    • C09K3/1012—Sulfur-containing polymers, e.g. polysulfides
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
    • C08L71/02—Polyalkylene oxides
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L81/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing sulfur with or without nitrogen, oxygen or carbon only; Compositions of polysulfones; Compositions of derivatives of such polymers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L81/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing sulfur with or without nitrogen, oxygen or carbon only; Compositions of polysulfones; Compositions of derivatives of such polymers
    • C08L81/04—Polysulfides
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D171/00—Coating compositions based on polyethers obtained by reactions forming an ether link in the main chain; Coating compositions based on derivatives of such polymers
    • C09D171/02—Polyalkylene oxides
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
    • C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
    • C08L2666/14—Macromolecular compounds according to C08L59/00 - C08L87/00; Derivatives thereof
    • C08L2666/22—Macromolecular compounds not provided for in C08L2666/16 - C08L2666/20

Definitions

  • the present invention relates to an improved one-part, non-curing sealant composition.
  • non-curing sealant compositions include chromates, with some compositions having up to 24% chromates by weight.
  • Use of chromates, particularly in large amounts, is hazardous and environmentally unfriendly.
  • a non- curing sealant composition which includes a monoepoxy compound, a polysulfide polymer, and a tertiary amine catalyst.
  • the composition is substantially free of chromates.
  • the inventive composition remains in an uncured state after exposure to a temperature of 250°F for 1000 hours.
  • the monoepoxy compound is a C 2 . 6 alkyl glycidyl ether, in particular butyl glycidyl ether.
  • the inventive composition also preferably includes one or more additives selected from the group consisting of fillers and salt corrosion inhibitors, and also preferably includes a solvent, such as ethyl acetate.
  • the inventive composition further includes a liquid polythioether polymer having a functionality between about 2 and about 3. More specifically, when the liquid polythioether polymer is included, the polysulfide is a non-reactive alkyl polysulfide.
  • a method of making a non-curing sealant composition comprising the steps of: forming a mixture by combining a monoepoxy compound, a polysulfide polymer, and a tertiary amine catalyst, the mixture being substantially free of chromates; and heating the mixture at a temperature of at least about 1 60°F for a time sufficient to afford a mercaptan equivalent weight of not less than 1 2,000.
  • a liquid polythioether polymer having a functionality between about 2 and about 3 is included in the mixture.
  • the polysulfide polymer preferably is a non-reactive alkyl polysulfide polymer.
  • an additive selected from the group consisting of fillers and salt corrosion inhibitors is added to the mixture.
  • a solvent such as ethyl acetate, preferably is also added to the mixture after the second step.
  • the inventive composition is a one-part, non-curing sealant composition which includes a monoepoxy compound, a polysulfide polymer, preferably a high-molecular weight polysulfide polymer, and a tertiary amine catalyst.
  • the composition is substantially free of chromates.
  • substantially free of chromates means having an amount of chromates less than 0.1 wt%, based on the non-volatile components of the composition, and preferably about 0 wt%.
  • Chromers includes hexavalent chromium compounds including Group II compounds such as calcium,, barium and strontium chromates, as well as other chromates such as zinc chromate.
  • a "one-part sealant” denotes a sealant that is used or applied without requiring the addition of an additional ingredient prior to use.
  • a “non-curing sealant” denotes a sealant that remains in an uncured state after application. Preferably, the inventive composition remains in an uncured state after exposure to a temperature of 250°F for 1000 hours. The following test is employed to determine whether a given sealant is non-curing: a layer of the sealant to be tested is applied to an aluminum panel having the dimensions 40 mil x 3 inch x 6 inch. The sealant is applied in a layer having a thickness of 20 to 40 mils, a width of 1 to 2 inches and a length of 3 to 4 inches.
  • Monoepoxy compounds useful according to the invention include alkyl and aryl glycidyl ethers, which may be further substituted with non-reactive and non-hindering groups.
  • Preferred compounds include C 2 . 6 alkyl glycidyl ethers, in particular butyl glycidyl ether, and aryl glycidyl ethers such as phenyl glycidyl ether.
  • the monoepoxy compound preferably is present in the composition in an amount from about 0.5 to about 10 wt%.
  • the inventive composition also includes a polysulfide polymer, preferably a high molecular weight polysulfide polymer.
  • a "high molecular weight polysulfide polymer” denotes a polysulfide type polymer having a molecular weight greater than about 20,000 Daltons. The high molecular weight polysulfide polymer improves the fuel resistance of the composition.
  • Exemplary polysulfides useful in the inventive composition include type MX and type WD-6 polysulfide polymers.
  • the composition includes about 10 to about 90 wt% of the selected polysulfide(s).
  • Useful tertiary amine catalysts for the inventive composition include diethylenetriamine (DET), 1 ,4-diaza-bicyclo[2.2.2]octane (DABCO ® , commercially available from Air Products, Chemical Additives Division, Allentown, Pennsylvania) and DMP-30 ® (an accelerant composition including 2,4,6- tri(dimethylaminomethyl)phenol, commercially available from Rohm and Haas. Philadelphia, Pennsylvania). Other known tertiary amine catalysts can also be used if desired.
  • DET diethylenetriamine
  • DABCO ® 1 ,4-diaza-bicyclo[2.2.2]octane
  • DMP-30 ® an accelerant composition including 2,4,6- tri(dimethylaminomethyl)phenol, commercially available from Rohm and Haas. Philadelphia, Pennsylvania.
  • Other known tertiary amine catalysts can also be used if desired.
  • the inventive composition includes about 0.01 to about 2 wt%, preferably about 0.2 to about 0.3 wt%, of the selected tertiary amine catalyst(s).
  • the inventive composition also includes a liquid polythioether polymer having a functionality between about 2 and about 3, that is, between about 2 and about 3 reactive groups per polymer molecule.
  • a liquid polythioether polymer having a functionality between about 2 and about 3, that is, between about 2 and about 3 reactive groups per polymer molecule.
  • liquid polythioether polymers can also be used if desired.
  • the number average molecular weight of the selected liquid polythioether polymer(s) ranges from about 500 to about 20,000, preferably from about 1 ,000 to about
  • the inventive sealant composition includes up to about 90 wt%, preferably about 10 to about 90 wt%, of the selected liquid polythioether polymer. Mixtures of two or more polymers can also be used if desired.
  • the monoepoxy compound preferably is present in the composition in the proportion from about 1 : 1 to about 1 : 1 .1 5, preferably about 1 .1 to about 1 :1.05, based on the number of moles of liquid polythioether polymer(s) present in the composition. Below this range, excess free mercaptan groups will be present and will result in oxidation and skin formation (due to formation of disulfide linkages). Above this range, excess epoxy will be present and may self-react.
  • the polysulfide polymer is a non-reactive alkyl polysulfide.
  • the composition further includes a solvent or mixture of solvents to improve the brushability of the composition.
  • solvents include lower alkyl (e.g., C, ⁇ ) esters, for example ethyl acetate, lower alkyl ketones such as acetone, methyl ethyl ketone, etc.,, aromatic solvents such as xylene and toluene, ethers such as dioxane, etc.
  • the composition includes about 0.05 to about 10%, more preferably about 3 to about 10 wt%, of the solvent or solvents, with the amount of solvent being based on the total weight of the composition.
  • the inventive composition also includes about 1 to about 30 wt% of at least one additive selected from the group consisting of fillers and salt corrosion inhibitors.
  • Fillers useful in the inventive compositions include water-ground mica and silica. Other known fillers can also be used.
  • Useful salt corrosion inhibitors include calcium strontium zinc phosphosilicate; (2-benzothiazolylthio)succinic acid, titanium dioxide, and zinc orthophosphate. Other useful salt corrosion inhibitors are disclosed in copending U.S. Patent Application Serial No.08/731 , 066, which is incorporated herein by reference.
  • the sealant compositions according to the invention have excellent resistance to aviation fuel. Resistance to aviation fuel can be quantified according to the following method: a layer of the sealant composition having a thickness of 20 mils (0.020 inch) is applied to a surface. The surface is immersed in a vertical orientation in jet reference fluid (JRF) type 1 at a temperature of 1 60°F for 48 hours. The composition is resistant to aviation fuel for the purposes of this invention if a maximum downward flow or "sag" of 2 mm (0.1 inch) is measured.
  • JRF jet reference fluid
  • JRF type 1 as employed herein for determination of fuel resistance, has the following composition (see AMS 2629, issued July 1 , 1989), section 3.1 .1 et seq., available from SAE (Society of Automotive Engineers, Warrendale, PA): Toluene 28 ⁇ 1 % by volume
  • compositions can be prepared according to the following method.
  • a mixture is formed by combining a monoepoxy compound, a polysulfide polymer, a tertiary amine catalyst as described herein, and .optionally a liquid polythioether polymer having a functionality between about 2 and about 3, the mixture being substantially free of chromates.
  • the mixture so formed is heated at a temperature of at least about 1 0°F for a time sufficient to afford a mercaptan equivalent weight of not less than 1 2,000, more preferably not less than 1 6,000, very preferably not less than 20,000.
  • the mercaptan equivalent is a measure of the extent of conversion of the thiol-terminated polymer (e.g., the polysulfide and/or the polythioether polymer), that is, the extent of reaction between the polymer and the monoepoxy compound.
  • a mercaptan equivalent of 1 2,000 indicates that one mercaptan equivalent is present per 12,000 g of polymer.
  • Mercaptan equivalent can be determined by conventional methods such as iodine titration.
  • the heating step is preferably carried out at a temperature of at least about 140°F, preferably about 140 to about 200°F, more preferably about 160 to about 180°F, very preferably about 160°F.
  • the upper limit on the temperature will be that temperature at which the selected monoepoxy compound begins to self-react.
  • the heating step preferably is carried out for a time from about 12 to about 48 hours, depending on the ingredients selected for use in the composition.
  • an additive selected from the group consisting of fillers and salt corrosion inhibitors is added to the mixture.
  • a solvent such as ethyl acetate, preferably is also added to the mixture after the second step.
  • inventive compositions are useful in a variety of applications, including without limitation control system joints, wet installed bushings, protection of landing gear metals, seat tracks, main rotors and rear rotor assemblies, transmission assemblies and protection of dissimilar or similar metals with easy disassembly.
  • Example 1 a liquid polythioether polymer was first prepared according to the methods described in copending U.S. Patent Application Serial No. 08/802,1 30 and Serial No. 08/928,972, incorporated herein in their entireties by reference.
  • Other polythioether polymers can also be used, and the present invention is not limited to the use of such polymers.
  • Example 1

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Sealing Material Composition (AREA)
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Abstract

A non-curing sealant composition includes a monoepoxy compound, a polysulfide, and a tertiary amine catalyst, and optionally a liquid polythioether polymer having a functionality between about 2 and about 3. The composition is substantially free of chromates.

Description

CHROMATE-FREE, ONE-PART, NON-CURING CORROSION INHIBITIVE SEALANT WITH RESISTANCE TO AVIATION FUEL
Field of the Invention The present invention relates to an improved one-part, non-curing sealant composition.
Background of the Invention Most known one-part, non-curing sealant compositions include chromates, with some compositions having up to 24% chromates by weight. Use of chromates, particularly in large amounts, is hazardous and environmentally unfriendly.
Furthermore, curing eventually occurs in such compositions with long-term exposure to high temperatures (240°F and higher). Such compositions also tend to wash off the surfaces to which they are applied when they are exposed to aviation fuel at temperatures of 140°F and higher. A need exists for an improved one-part, non-curing sealant that avoids the foregoing problems.
Summary of the Preferred Embodiments In accordance with one aspect of the present invention, there is provided a non- curing sealant composition which includes a monoepoxy compound, a polysulfide polymer, and a tertiary amine catalyst. The composition is substantially free of chromates.
Preferably, the inventive composition remains in an uncured state after exposure to a temperature of 250°F for 1000 hours.
In a preferred embodiment, the monoepoxy compound is a C2.6 alkyl glycidyl ether, in particular butyl glycidyl ether.
The inventive composition also preferably includes one or more additives selected from the group consisting of fillers and salt corrosion inhibitors, and also preferably includes a solvent, such as ethyl acetate.
In a preferred embodiment, the inventive composition further includes a liquid polythioether polymer having a functionality between about 2 and about 3. More specifically, when the liquid polythioether polymer is included, the polysulfide is a non-reactive alkyl polysulfide.
In accordance with another aspect of the present invention, there is provided a method of making a non-curing sealant composition comprising the steps of: forming a mixture by combining a monoepoxy compound, a polysulfide polymer, and a tertiary amine catalyst, the mixture being substantially free of chromates; and heating the mixture at a temperature of at least about 1 60°F for a time sufficient to afford a mercaptan equivalent weight of not less than 1 2,000.
In a preferred embodiment, in the first step a liquid polythioether polymer having a functionality between about 2 and about 3 is included in the mixture. In this embodiment, the polysulfide polymer preferably is a non-reactive alkyl polysulfide polymer.
Preferably, after the second step of the method, an additive selected from the group consisting of fillers and salt corrosion inhibitors is added to the mixture. A solvent, such as ethyl acetate, preferably is also added to the mixture after the second step.
Other objects, features and advantages of the present invention will become apparent to those skilled in the art from the following detailed description. It is to be understood, however, that the detailed description and specific examples, while indicating preferred embodiments of the present invention, are given by way of illustration and not limitation. Many changes and modifications within the scope of the present invention may be made without departing from the spirit thereof, and the invention includes all such modifications.
Detailed Description of the Preferred Embodiments The inventive composition is a one-part, non-curing sealant composition which includes a monoepoxy compound, a polysulfide polymer, preferably a high-molecular weight polysulfide polymer, and a tertiary amine catalyst. The composition is substantially free of chromates.
The term "substantially free of chromates" means having an amount of chromates less than 0.1 wt%, based on the non-volatile components of the composition, and preferably about 0 wt%. "Chromates" includes hexavalent chromium compounds including Group II compounds such as calcium,, barium and strontium chromates, as well as other chromates such as zinc chromate.
As used herein, a "one-part sealant" denotes a sealant that is used or applied without requiring the addition of an additional ingredient prior to use. As used herein, a "non-curing sealant" denotes a sealant that remains in an uncured state after application. Preferably, the inventive composition remains in an uncured state after exposure to a temperature of 250°F for 1000 hours. The following test is employed to determine whether a given sealant is non-curing: a layer of the sealant to be tested is applied to an aluminum panel having the dimensions 40 mil x 3 inch x 6 inch. The sealant is applied in a layer having a thickness of 20 to 40 mils, a width of 1 to 2 inches and a length of 3 to 4 inches. The coated aluminum panel is then exposed to dry heat at 1 1 5-1 20°C (about 240-250°F) for 1000 hours. The sealant should still be tacky and easy to remove from the panel at the end of exposure. Monoepoxy compounds useful according to the invention include alkyl and aryl glycidyl ethers, which may be further substituted with non-reactive and non-hindering groups. Preferred compounds include C2.6 alkyl glycidyl ethers, in particular butyl glycidyl ether, and aryl glycidyl ethers such as phenyl glycidyl ether. The monoepoxy compound preferably is present in the composition in an amount from about 0.5 to about 10 wt%.
The inventive composition also includes a polysulfide polymer, preferably a high molecular weight polysulfide polymer. As used herein, a "high molecular weight polysulfide polymer" denotes a polysulfide type polymer having a molecular weight greater than about 20,000 Daltons. The high molecular weight polysulfide polymer improves the fuel resistance of the composition.
Exemplary polysulfides useful in the inventive composition include type MX and type WD-6 polysulfide polymers. Preferably, the composition includes about 10 to about 90 wt% of the selected polysulfide(s).
Useful tertiary amine catalysts for the inventive composition include diethylenetriamine (DET), 1 ,4-diaza-bicyclo[2.2.2]octane (DABCO®, commercially available from Air Products, Chemical Additives Division, Allentown, Pennsylvania) and DMP-30® (an accelerant composition including 2,4,6- tri(dimethylaminomethyl)phenol, commercially available from Rohm and Haas. Philadelphia, Pennsylvania). Other known tertiary amine catalysts can also be used if desired.
Preferably the inventive composition includes about 0.01 to about 2 wt%, preferably about 0.2 to about 0.3 wt%, of the selected tertiary amine catalyst(s).
In a specific preferred embodiment, the inventive composition also includes a liquid polythioether polymer having a functionality between about 2 and about 3, that is, between about 2 and about 3 reactive groups per polymer molecule. Useful liquid polythioether polymers according to the invention include those described in copending, commonly assigned U.S. Patent Applications Serial No. 08/802,130, filed
February 1 9, 1 997, and Serial No. 08/928,972, filed September 12, 1997; U.S. Patent No. 4,366,307 to Singh et al.; and U.S. Patent No. 4,609,762, to Morris et al. Other liquid polythioether polymers can also be used if desired. Preferably, the number average molecular weight of the selected liquid polythioether polymer(s) ranges from about 500 to about 20,000, preferably from about 1 ,000 to about
10,000, very preferably about 2,000 to about 5,000.
Preferably, the inventive sealant composition includes up to about 90 wt%, preferably about 10 to about 90 wt%, of the selected liquid polythioether polymer. Mixtures of two or more polymers can also be used if desired. When the liquid polythioether polymers are used, the monoepoxy compound preferably is present in the composition in the proportion from about 1 : 1 to about 1 : 1 .1 5, preferably about 1 .1 to about 1 :1.05, based on the number of moles of liquid polythioether polymer(s) present in the composition. Below this range, excess free mercaptan groups will be present and will result in oxidation and skin formation (due to formation of disulfide linkages). Above this range, excess epoxy will be present and may self-react.
In a more specific embodiment, when the liquid polythioether polymer is used, the polysulfide polymer is a non-reactive alkyl polysulfide.
In the foregoing description of the preferred quantities of the various ingredients of the composition, all wt% are based on the non-volatile components of the composition.
Preferably, the composition further includes a solvent or mixture of solvents to improve the brushability of the composition. Useful solvents include lower alkyl (e.g., C,^) esters, for example ethyl acetate, lower alkyl ketones such as acetone, methyl ethyl ketone, etc.,, aromatic solvents such as xylene and toluene, ethers such as dioxane, etc. Preferably the composition includes about 0.05 to about 10%, more preferably about 3 to about 10 wt%, of the solvent or solvents, with the amount of solvent being based on the total weight of the composition.
Preferably, the inventive composition also includes about 1 to about 30 wt% of at least one additive selected from the group consisting of fillers and salt corrosion inhibitors.
Fillers useful in the inventive compositions include water-ground mica and silica. Other known fillers can also be used.
Useful salt corrosion inhibitors include calcium strontium zinc phosphosilicate; (2-benzothiazolylthio)succinic acid, titanium dioxide, and zinc orthophosphate. Other useful salt corrosion inhibitors are disclosed in copending U.S. Patent Application Serial No.08/731 , 066, which is incorporated herein by reference. The sealant compositions according to the invention have excellent resistance to aviation fuel. Resistance to aviation fuel can be quantified according to the following method: a layer of the sealant composition having a thickness of 20 mils (0.020 inch) is applied to a surface. The surface is immersed in a vertical orientation in jet reference fluid (JRF) type 1 at a temperature of 1 60°F for 48 hours. The composition is resistant to aviation fuel for the purposes of this invention if a maximum downward flow or "sag" of 2 mm (0.1 inch) is measured.
JRF type 1 , as employed herein for determination of fuel resistance, has the following composition (see AMS 2629, issued July 1 , 1989), section 3.1 .1 et seq., available from SAE (Society of Automotive Engineers, Warrendale, PA): Toluene 28 ± 1 % by volume
Cyclohexane (technical) 34 ± 1 % by volume
Isooctane 38 ± 1 % by volume
Tertiary dibutyl disulfide (doctor sweet) 1 ± 0.005% by volume
Tertiary butyl mercaptan 0.01 5% ± 0.001 5 by weight of the other four components
The inventive compositions can be prepared according to the following method. In a first step, a mixture is formed by combining a monoepoxy compound, a polysulfide polymer, a tertiary amine catalyst as described herein, and .optionally a liquid polythioether polymer having a functionality between about 2 and about 3, the mixture being substantially free of chromates. Next, the mixture so formed is heated at a temperature of at least about 1 0°F for a time sufficient to afford a mercaptan equivalent weight of not less than 1 2,000, more preferably not less than 1 6,000, very preferably not less than 20,000.
As known to those skilled in the art, the mercaptan equivalent is a measure of the extent of conversion of the thiol-terminated polymer (e.g., the polysulfide and/or the polythioether polymer), that is, the extent of reaction between the polymer and the monoepoxy compound. A mercaptan equivalent of 1 2,000 indicates that one mercaptan equivalent is present per 12,000 g of polymer. Mercaptan equivalent can be determined by conventional methods such as iodine titration.
The heating step is preferably carried out at a temperature of at least about 140°F, preferably about 140 to about 200°F, more preferably about 160 to about 180°F, very preferably about 160°F. The upper limit on the temperature will be that temperature at which the selected monoepoxy compound begins to self-react.
The heating step preferably is carried out for a time from about 12 to about 48 hours, depending on the ingredients selected for use in the composition.
Preferably, after the second step of the method, an additive selected from the group consisting of fillers and salt corrosion inhibitors is added to the mixture. A solvent, such as ethyl acetate, preferably is also added to the mixture after the second step.
The inventive compositions are useful in a variety of applications, including without limitation control system joints, wet installed bushings, protection of landing gear metals, seat tracks, main rotors and rear rotor assemblies, transmission assemblies and protection of dissimilar or similar metals with easy disassembly.
The invention is further illustrated by the following non-limiting examples. In Example 1 , a liquid polythioether polymer was first prepared according to the methods described in copending U.S. Patent Application Serial No. 08/802,1 30 and Serial No. 08/928,972, incorporated herein in their entireties by reference. Other polythioether polymers can also be used, and the present invention is not limited to the use of such polymers. Example 1
In a 2 liter flask, 524.8g (3.32 mole) of diethylene glycol divinyl ether (DEG- DVE) and 706.7g (3.87 mole) of dimercaptodioxaoctane (DMDO) were mixed with 1 9.7 g (0.08 mole) of triallylcyanurate (TAC) and heated to 77°C. To the heated reaction mixture was added 4.6 g (0.024 mole) of an azobisnitrile free radical catalyst
(VAZO®67 [2,2'- azobis (2-methylbutyronitrile)], commercially available from DuPont). The reaction proceeded substantially to completion after 2 hours to afford 1 250 g (0.39 mole, yield 100%) of a liquid polythioether resin having a Tg of -68°C and a viscosity of 65 poise. The resin was faintly yellow and had a low color. Next, 100 grams (0.069 equivalents) of the foregoing thiol terminated polythioether polymer, 9.0 grams (0.069 equivalents) of butyl glycidyl ether and 0.05 grams of diazabicyclooctane were mixed together and heated at 160°F until a mercaptan equivalent weight of 1 2,000 grams/equivalent or greater was reached. To this mixture were added 2 grams of WD-6 polysulfide polymer (mercaptan equivalent weight > 1 2,000 grams/equivalent, commercially available from Morton
Adhesives and Chemical Specialties, Chicago, III.), 10 grams of water ground mica and 1 0 grams of zinc orthophosphate. The entire mixture was vigorously agitated until the filler particles were thoroughly and homogeneously dispersed.
The resulting sealant was spread on an aluminum dish and heated in a recirculating air oven for 2 weeks at 200° F. No evidence of curing or skinning was noted. Example 2
100 Grams (0.034 equivalents) of a 50:50 blend of WD-6 and LP-2 polysulfide polymer (both available from Morton Adhesives and Chemical Specialties), 4.5 grams (0.034 equivalents) of butyl glycidyl ether and 0.05 grams of diazabicyclooctane are mixed together and heated at 1 60°F until a mercaptan equivalent weight of 18,000 grams/equivalent or greater was reached. To this mixture were added 10 grams of titanium dioxide and 10 grams of zinc orthophosphate. The entire mixture was vigorously agitated until the filler particles were thoroughly and homogeneously dispersed. The resulting sealant was spread on an aluminum dish and heated in a recirculating air oven for 2 weeks at 200° F. No evidence of curing or skinning was noted. The sealant was spread on an aluminum panel and immersed in a 3.5% NaCI water solution for 7 days. Upon removal of the sealant, no evidence of corrosion was observed.

Claims

What is claimed:
1 . A non-curing sealant composition comprising
(a) a monoepoxy compound,
(b) a polysulfide, and
(c) a tertiary amine catalyst, said composition being substantially free of chromates.
2. The composition of claim 1 which remains in an uncured state after exposure to a temperature of 250°F for 1000 hours.
3. The composition of claim 1 having a mercaptan equivalent of at least 1 2,000.
4. The composition of claim 1 wherein said monoepoxy compound is a C2.6 alkyl glycidyl ether.
5. The composition of claim 4 wherein said monoepoxy compound is butyl glycidyl ether.
6. The composition of claim 1 wherein said monoepoxy compound is an aryl glycidyl ether.
7. The composition of claim 6 wherein said monoepoxy compound is phenyl glycidyl ether.
8. The composition of claim 1 further comprising (d) a liquid polythioether polymer having a functionality between about 2 and about 3.
9. The composition of claim 8 wherein said liquid polythioether polymer has a number average molecular weight ranging from about 500 to about 20,000.
10. The composition of claim 8 comprising a plurality of said liquid polythioether polymers.
1 1 . The composition of claim 8 wherein the molar ratio of ingredient (d) to ingredient (a) ranges from about 1 :1 to about 1 : 1 5.
12. The composition of claim 8 wherein said polysulfide is a non-reactive alkyl polysulfide.
13. The composition of claim 1 further comprising an additive selected from the group consisting of fillers and salt corrosion inhibitors.
1 . The composition of claim 1 further comprising a solvent.
1 5. The composition of claim 14 wherein said solvent is ethyl acetate.
16. A non-puring sealant composition comprising
(a) about 0 to about 90 wt% of a liquid polythioether polymer having a functionality between about 2 and about 3,
(b) about 0.5 to about 10 wt% of a monoepoxy compound,
(c) about 10 to about 90 wt% of a non-reactive alkyl polysulfide, and
(d) about 0.01 to about 2 wt% of a tertiary amine catalyst, wherein all wt% are based on the non-volatile components of the composition, said composition being substantially free of chromates.
17. The composition of claim 16 comprising about 10 to about 90 wt% of ingredient (a).
18. The composition of claim 16 further comprising about 0.05 to about 10 wt% of a solvent.
19. The composition of claim 16 further comprising about 1 to about 30 wt% of at least one additive selected from the group consisting of fillers and salt corrosion inhibitors.
20. A method of making a non-curing sealant composition comprising the steps of
(i) forming a mixture by combining
(a) a monoepoxy compound,
(b) a polysulfide, and
(c) a tertiary amine catalyst, said mixture being substantially free of chromates, and (ii) heating said mixture at a temperature of at least about 1 60°F for a time sufficient to afford a mercaptan equivalent weight of not less than 12,000.
21 . The method of claim 20 wherein in step (i) said mixture further comprises (d) a liquid polythioether polymer having a functionality between about 2 and about 3.
22. The method of claim 21 wherein in step (i) said polysulfide is a non- reactive alkyl polysulfide.
23. The method of claim 21 wherein after step (ii) an additive selected from the group consisting of fillers and salt corrosion inhibitors is added to said mixture.
24. The method of claim 21 wherein after step (ii) a solvent is added to said mixture.
PCT/US1998/023655 1997-11-07 1998-11-06 Chromate-free, one-part, non-curing corrosion inhibitive sealant with resistance to aviation fuel WO1999024491A1 (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
JP2000520496A JP4157276B2 (en) 1997-11-07 1998-11-06 Chromate-free, one-part, non-curing, corrosion-resistant sealant that is resistant to aviation fuels
CA002309211A CA2309211C (en) 1997-11-07 1998-11-06 Chromate-free, one-part, non-curing corrosion inhibitive sealant with resistance to aviation fuel
DE69806046T DE69806046T2 (en) 1997-11-07 1998-11-06 CHROMATE-FREE, NON-HARDENING, CORROSION-PROOF INCOMPONENT INSULATING AGENT, RESISTANT TO FLUX BIN
EP98963753A EP1032607B1 (en) 1997-11-07 1998-11-06 Chromate-free, one-part, non-curing corrosion inhibitive sealant with resistance to aviation fuel
BR9813979-7A BR9813979A (en) 1997-11-07 1998-11-06 Non-curable, single-component, chromate-free corrosion inhibitor seal with resistance to aviation fuels and method for its preparation
AU19011/99A AU736628B2 (en) 1997-11-07 1998-11-06 Chromate-free, one-part, non-curing corrosion inhibitive sealant with resistance to aviation fuel
KR1020007004841A KR20010031775A (en) 1997-11-07 1998-11-06 Chromate-free, one-part, non-curing corrosion inhibitive sealant with resistance to aviation fuel

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US6494197P 1997-11-07 1997-11-07
US60/064,941 1997-11-07

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AU (1) AU736628B2 (en)
BR (1) BR9813979A (en)
CA (1) CA2309211C (en)
DE (1) DE69806046T2 (en)
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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004529238A (en) * 2001-04-06 2004-09-24 ヒェメタル ゲゼルシャフト ミット ベシュレンクテル ハフツング Low-density encapsulant, base material and method for its production and use
WO2006029145A2 (en) * 2004-09-08 2006-03-16 Prc-Desoto International, Inc. Preformed compositions in shaped form comprising polymer blends
WO2006029144A1 (en) * 2004-09-08 2006-03-16 Prc-Desoto International, Inc. Polymer blend and compositions and methods for using the same
US7553908B1 (en) 2003-01-30 2009-06-30 Prc Desoto International, Inc. Preformed compositions in shaped form comprising polymer blends
WO2017074919A1 (en) * 2015-10-26 2017-05-04 Prc-Desoto International, Inc. Non-chromate corrosion inhibiting polythioether sealants
EP3719097A4 (en) * 2017-11-29 2021-07-28 Nitto Denko Corporation Sealant sheet

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001066642A1 (en) 2000-03-09 2001-09-13 Pbt Brands, Inc. Sealants containing multimodal polymer blends
MXPA02008811A (en) 2000-03-09 2004-10-14 Advanced Chemistry And Technol High strength polymers and aerospace sealants therefrom.
US6242618B1 (en) * 2000-03-21 2001-06-05 The Lubrizol Corporation H2S scavengers for polysulfide products and methods for scavenging H2S from polysulfide products
US7229700B2 (en) * 2004-10-26 2007-06-12 Basf Catalysts, Llc. Corrosion-resistant coating for metal substrate
DE102005039987A1 (en) * 2005-08-23 2007-03-01 Bartels Mikrotechnik Gmbh Steam iron, has pump, which provides connection between fluid reservoir and steam chamber, and is arranged, designed, dimensioned and accesses such that desired amount of water is transported from reservoir into chamber
US20070096396A1 (en) * 2005-10-27 2007-05-03 Sawant Suresh G Dimercaptan terminated polythioether polymers and methods for making and using the same
US9771483B2 (en) * 2013-04-19 2017-09-26 The Boeing Company Systems, compositions, and methods for corrosion inhibition

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4017554A (en) * 1973-07-06 1977-04-12 Thiokol Corporation Epoxide modified polysulfide polymers as adhesive additives for liquid polysulfide polymer based adhesive compositions
US4153743A (en) * 1977-03-29 1979-05-08 Caramanian John A Concrete surface treating material and method of treating concrete surfaces
US4366307A (en) * 1980-12-04 1982-12-28 Products Research & Chemical Corp. Liquid polythioethers
US4692500A (en) * 1986-07-07 1987-09-08 The Dow Chemical Company Polysulfide modified epoxy resins
US5610243A (en) * 1993-12-20 1997-03-11 Morton International, Inc. Polysulfide-epoxy thermoplastic elastomers

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4595714A (en) * 1981-03-13 1986-06-17 Fiber Materials, Inc. Ablative coating composition and product
US4656095A (en) * 1984-05-31 1987-04-07 Fiber Materials, Inc. Ablative composition
WO1986007369A1 (en) * 1985-06-11 1986-12-18 Products Research And Chemical Corporation Method of producing mercaptan terminated polymers with increased reactivity and reduced odor
EP0304948B1 (en) * 1987-08-28 1994-06-01 Nec Corporation Data processor including testing structure for barrel shifter
WO1989008129A1 (en) * 1988-02-26 1989-09-08 Sandoz Ag Improvements in or relating to organic compounds
US4983692A (en) * 1989-01-23 1991-01-08 The Dow Chemical Company Sulfide containing aliphatic epoxy resins
AU633152B2 (en) * 1989-10-18 1993-01-21 Toray Thiokol Company Limited Polysulfide polyether, method of producing same, polymer composition and curable composition
US5494729A (en) * 1992-05-20 1996-02-27 Impact Coatings, Inc. Non-slip, non-abrasive coated surface

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4017554A (en) * 1973-07-06 1977-04-12 Thiokol Corporation Epoxide modified polysulfide polymers as adhesive additives for liquid polysulfide polymer based adhesive compositions
US4153743A (en) * 1977-03-29 1979-05-08 Caramanian John A Concrete surface treating material and method of treating concrete surfaces
US4366307A (en) * 1980-12-04 1982-12-28 Products Research & Chemical Corp. Liquid polythioethers
US4692500A (en) * 1986-07-07 1987-09-08 The Dow Chemical Company Polysulfide modified epoxy resins
US5610243A (en) * 1993-12-20 1997-03-11 Morton International, Inc. Polysulfide-epoxy thermoplastic elastomers

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004529238A (en) * 2001-04-06 2004-09-24 ヒェメタル ゲゼルシャフト ミット ベシュレンクテル ハフツング Low-density encapsulant, base material and method for its production and use
US7553908B1 (en) 2003-01-30 2009-06-30 Prc Desoto International, Inc. Preformed compositions in shaped form comprising polymer blends
WO2006029145A3 (en) * 2004-09-08 2006-04-27 Prc Desoto Int Inc Preformed compositions in shaped form comprising polymer blends
WO2006029144A1 (en) * 2004-09-08 2006-03-16 Prc-Desoto International, Inc. Polymer blend and compositions and methods for using the same
AU2005282552B2 (en) * 2004-09-08 2008-09-11 Prc-Desoto International, Inc. Polymer blend and compositions and methods for using the same
KR100887788B1 (en) * 2004-09-08 2009-03-09 피알시-데소토 인터내쇼날, 인코포레이티드 Preformed compositions in shaped form comprising polymer blends
WO2006029145A2 (en) * 2004-09-08 2006-03-16 Prc-Desoto International, Inc. Preformed compositions in shaped form comprising polymer blends
KR100934051B1 (en) * 2004-09-08 2009-12-24 피알시-데소토 인터내쇼날, 인코포레이티드 Polymer Blends, Compositions, and Methods of Use thereof
EP2239300A1 (en) * 2004-09-08 2010-10-13 Prc-Desoto International, Inc. Polymer blend and compositions and methods for using the same
WO2017074919A1 (en) * 2015-10-26 2017-05-04 Prc-Desoto International, Inc. Non-chromate corrosion inhibiting polythioether sealants
US10053606B2 (en) 2015-10-26 2018-08-21 Prc-Desoto International, Inc. Non-chromate corrosion inhibiting polythioether sealants
RU2697663C1 (en) * 2015-10-26 2019-08-16 Прк-Десото Интернэшнл, Инк. Non-chromate corrosion-inhibiting sealants based on polythioether
EP3719097A4 (en) * 2017-11-29 2021-07-28 Nitto Denko Corporation Sealant sheet
US11891506B2 (en) 2017-11-29 2024-02-06 Nitto Denko Corporation Sealant sheet

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CA2309211A1 (en) 1999-05-20
ES2174529T3 (en) 2002-11-01
DE69806046T2 (en) 2003-02-06
AU1901199A (en) 1999-05-31
KR20010031775A (en) 2001-04-16
JP2001522910A (en) 2001-11-20
EP1032607A1 (en) 2000-09-06
US6069211A (en) 2000-05-30
EP1032607B1 (en) 2002-06-12
CN1134489C (en) 2004-01-14
JP4157276B2 (en) 2008-10-01
CA2309211C (en) 2008-09-02
AU736628B2 (en) 2001-08-02
CN1281479A (en) 2001-01-24
BR9813979A (en) 2000-09-26
EP1032607A4 (en) 2001-02-07
DE69806046D1 (en) 2002-07-18

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