Rapidly curing adhesives using encapsulated catalyst and focused ultrasound

Patent metadata

Field	Value
Publication number	US-10246565-B2
Application number	US-201514667220-A
Country	US
Kind code	B2
Filing date	Mar 24, 2015
Priority date	Mar 24, 2015
Publication date	Apr 2, 2019
Grant date	Apr 2, 2019

Abstract

Methods for making and curing resin-based adhesives are disclosed using encapsulated amine accelerators activated by providing ultrasonic energy.

First claim

What is claimed is:

1. A method for making an on-demand adhesive comprising the steps of:
mixing a resin-based compound with a non-gas-filled encapsulated catalyst to form an uncured resin-based adhesive,
depositing said uncured resin-based adhesive onto component, said catalyst encapsulated within a shell, said shell having an average shell diameter of from about 1 to about 1000 microns, and said shell having an average shell wall thickness of from about 1 to about 10% of the shell diameter;
directing non-thermal ultrasonic energy from an ultrasonic energy source through the component, said ultrasonic energy source emitting ultrasonic energy from a curved piezoelectric ceramic probe head with the emitted ultrasonic energy tuned to an ultrasonic energy in the range of from about 0.5 to about 50 MHz;
focusing the non-thermal ultrasonic energy through the component to a region or point located in the deposited adhesive;
targeting non-thermal ultrasonic energy frequencies corresponding to a natural resonant frequency of the shell;
rupturing the non-gas-filled encapsulated catalyst; and
curing on-demand the uncured resin-based adhesive.

2. The method of claim 1 , wherein the resin-based compound comprises an epoxy resin-based compound, and the encapsulated catalyst is a compound selected from the group consisting of: boron trichloride methyl amine, boron trichloride ethylamine, and homologues, boron trifluoride methyl amine, boron trifluoride ethylamine and homologues, boron trifluoride dimethylamine, boron trifluoride diethylamine, and homologues, boron trifluoride trimethylamine, boron trifluoride triethylamine, and homologues, boron trifluoride piperadine, boron trifluoride hexylamine, and combinations thereof.

3. The method of claim 1 , wherein the resin-based compound is an epoxy resin-based compound selected from the group comprising: diglycidyl ethers of bisphenol A; diglycidyl ethers of bisphenol F; N,N,N′,N′-tetraglycidyl-4,4′-diaminophenylmethane; p-amino phenol triglycidyl ether; epoxy phenol novolac resins; epoxy cresol novolac resins; 1,3,5-triglycidyl isocyanurate; tris(2,3-epoxypropyl)isocyanurate; glycerol diglycidyl ether; trimethylolpropane triglycidyl ether, and combinations thereof.

4. The method of claim 3 , wherein the step of mixing a resin-based compound with an encapsulated catalyst to form an uncured resin-based adhesive further comprising: mixing a thiol-based curing agent with the epoxy resin-based compound, wherein the thiol-based curing agent is selected from the group consisting of: pentaerythritol tetrakis(3-mercaptopropionate); trimethylolpropane tris(3-mercaptopropionate); 1,3,4-thiadiazole-2,5-dithiol; poly (ethylene glycol) dithiol; toluene dithiol; benzene dithiol; 1,2-ethanedithiol; tris[2-(3-mercaptopropionyloxy)ethyl] isocyanurate, other polyols grafted onto isocyanurate backbones and combinations thereof.

5. The method of claim 4 , wherein the encapsulated catalyst is selected from the group consisting of: N,N dimethyldodecyl amine and homologues; (1,8-Diazabicycloundec-7-ene); (1,5-diazabicyclo[4, 3, O]non-5-ene), trienthanolamine, piperazine, dimethylimidazol, 1-methylimidazole; nonylphenol; 1-(2-aminoethyl) piperazine, and combinations thereof.

6. The method of claim 1 , wherein the resin-based compound comprises an acrylate-based compound,
wherein the step of mixing a resin-based compound with an encapsulated catalyst to form an uncured resin-based adhesive further comprises mixing a thiol-based curing agent with the resin-based compound and encapsulated compound, and
wherein the thiol-based curing agent is selected from the group consisting of:
pentaerythritol tertrakis(3-mercaptopropionate); trimethylolpropane tris(3-mercaptopropionate); 1,3,4-thiadiazole-2,5-dithiol; poly(ethylene glycol) dithiol; toluene dithiol; benzene dithiol; 1,2-ethanedithiol; tris[2-(3-mercaptopropionyloxy)ethyl]isocyanurate other polyols grafted onto isocyanurate backbones, and combinations thereof.

7. The method of claim 6 , wherein the encapsulated catalyst is selected from the group consisting of: aliphatic primary amines, aliphatic secondary amines, and combinations thereof.

8. The method of claim 6 , wherein, the acrylate resin-based compound is selected from the group comprising: monoacrylates, diacrylates, triacrylates, tetraacrylates, pentaacrylates and combinations thereof.

9. A method for applying and curing an on-demand adhesive comprising the steps of:
mixing a resin-based compound with a non-gas-filled encapsulated catalyst to form an uncured adhesive material, said catalyst encapsulated within a shell, said shell having an average shell diameter of from about 1 to about 1000 microns, and said shell having an average shell wall thickness of from about 1 to about 10% of the shell diameter;
applying the uncured adhesive material onto an interior surface of a first component having an interior surface and an exterior surface;
positioning an ultrasonic energy source proximate to the exterior surface of the first component said first component having a thickness ranging from about 0.1 to about 0.25 inches;
directing non-thermal ultrasonic energy from an ultrasonic energy source through the first component and focused to a region or point in the uncured adhesive material applied onto the first component, said ultrasonic energy source emitting ultrasonic energy from a curved piezoelectric ceramic probe head with the emitted ultrasonic energy tuned to an ultrasonic energy in the range of from about 0.5 to about 50 MHz;
focusing the ultrasonic energy through the component to a region or point located in the deposited adhesive;
targeting ultrasonic energy frequencies corresponding to a natural resonant frequency of the shell;
rupturing the encapsulated catalyst; and
curing on-demand the uncured adhesive material.

10. The method of claim 9 , further comprising the step of: prior to directing ultrasonic energy, applying the uncured adhesive material onto an interior surface of a second component having an interior surface and an exterior surface substantially simultaneously with the step of applying the uncured adhesive material onto an interior surface of a first component having an interior surface and an exterior surface, said second component oriented proximate to the first component, such that a gap exists between the interior surface of the first component and the interior surface of the second component.

11. An uncured adhesive material, said uncured adhesive material comprising in a mixture: a resin-based compound; and a non-gas-filled encapsulated catalyst; wherein the catalyst is encapsulated within a shell, said shell having an average shell diameter of from about 1 to about 1000 microns, and said shell having an average shell wall thickness of from about 1 to about 10% of the shell diameter, and wherein the shell ruptures when a predetermined amount of energy is received by the shell from an ultrasonic energy source, said ultrasonic energy source configured to emit emitting ultrasonic energy from a curved piezoelectric ceramic probe head with the emitted ultrasonic energy tuned to an ultrasonic energy range of from about 0.5 to about 50 MHz, and wherein the uncured adhesive material is configured to be cured on-demand.

12. The adhesive material of claim 11 , wherein the resin-based compound comprises an epoxy resin-based compound, and the encapsulated catalyst is a compound selected from the group consisting of: boron trichloride methyl amine, boron trichloride ethylamine, and homologues, boron trifluoride methyl amine, boron trifluoride ethylamine and homologues, boron trifluoride dimethylamine, boron trifluoride diethylamine, and homologue

Assignees

• Boeing Co

Inventors

• Nowak Andrew P
• Mcknight Geoffrey P
• Pajel Carissa A
• Yang Sophia S
• Boundy Thomas I
• Rodriguez April R
• Hansen Darrin M
• Adjorlolo Alain A

Classifications

• B29K2307/04

  Carbon · CPC title

• B05D3/108

  Curing · CPC title

• B29C65/483

  Reactive adhesives, e.g. chemically curing adhesives · CPC title

• B29C66/1122

  Single lap to lap joints, i.e. overlap joints (B29C66/45, B29C66/472, B29C66/52272 take precedence) · CPC title

• C08F220/18

  with acrylic or methacrylic acids · CPC title