Process for preparation of self healing microcapsules

Patent metadata

Field	Value
Publication number	US-2016346753-A1
Application number	US-201615165522-A
Country	US
Kind code	A1
Filing date	May 26, 2016
Priority date	May 26, 2015
Publication date	Dec 1, 2016
Grant date	—

Abstract

The present invention disclosed a process for the preparation of microcapsules containing epoxy resin which comprises water-insoluble and/or water-soluble components prepared by in-situ polymerization using non-aqueous continuous phase which acts as healing agents for the micro-cracks when embedded in composite structures.

First claim

What is claimed is:

1 . A process for the preparation of self-healing microcapsules with polyurethane as capsule wall material prepared by in-situ polymerization using non-aqueous continuous phase comprising the steps of:
a) preparing a mixture of epoxy components to be encapsulated and polyisocyante; b) preparing a solution of diol or polyol with a cross-linker in aliphatic hydrocarbon; c) dispersing the mixture of step a) in a solution of a stabilizer and a catalyst in an aliphatic hydrocarbon; d) adding the solution of step (b) drop wise to the dispersion of step c) under agitation followed by treatment with anti-agglomerating agent to obtain microcapsules; and e) filtering and/or centrifuging, washing the microcapsules as obtained in step (d), with the aliphatic hydrocarbon and drying the microcapsules under vacuum at ambient temperature to obtain microcapsules with polyurethane as capsule wall material.

2 . The process as claimed in claim 1 , wherein said polyisocyante is selected from aromatic polyisocyanates, aliphatic polyisocyanates, or mixtures thereof and said aromatic polyisocyanate is selected from the group consisting of 2,4- and 2,6-toluene diisocyanate (TDI), naphthalene diisocyanate, diphenyl methane diisocyanate, triphenyl methane-p,p′p″-trityltriisocyanate, polymethylene polyphenyleneisocyanate, 2,4,4′-diphenylether triisocyanate, 3,3′-dimethyl-4,4′-diphenyl diisocyanate, 3,3′-dimethoxy-4,4′diphenyl diisocyanate, triphenylmethane 4,4′, 4″ triisocyanate, and mixtures thereof and said aliphatic polyisocyanate is selected from the group consisting of dicyclohexylmethane 4,4′-diisocyanate, hexamethylene1,6-diisocyanate (HMDI), isophoronediisocyanate (IPDI), trimethyl-hexamethylenediisocyanate, trimethylenediisocyanate, propylene-1,2-diisocyanate, butylene1,2-diisocyanate and mixtures thereof.

3 . The process as claimed in claim 1 , wherein said diol or polyol is selected from ethylene glycol, diethylene glycol, propylene glycol, 1,4-butane diol, 1,4 hexane diol, dipropylene glycol, cyclohexyl 1,4 dimethanol, 1,8 octane diol, 2,methyl 2,4 pentane diol (MPD), 1,3-propane diol, poly (ethylene glycols), poly (propylene glycols) or poly(tetra methylene glycols).

4 . The process as claimed in claim 1 , wherein said cross-linker is selected from the group consisting of butane-1,2,3-triol, butane-1,2,4-triol, 2,2-dihydromethyl-1,3propane diol, castor oil, caprolactone-based triols, 2-hydroxy methyl-1,3-propane diol, trimethylol propane (TMP), trimethylol ethane (TME) and mixtures thereof.

5 . The process as claimed in claim 1 , wherein said catalyst is selected from the group consisting of N, N′ dimethylaminoethanol, N, N′-dimethylcyclohexylamine, bis[2-(N,N′ dimethylamino)ethyl] ether, N,N′-dimethylacetylamine, diaminobicyclooctane, stannous octoate, dibutyltindilaurate (DBTDL) and mixtures thereof.

6 . A process for the preparation of self-healing microcapsules with epoxy as capsule wall material prepared by in-situ polymerization using non-aqueous continuous phase comprising the steps of:
a) dispersing epoxy components to be encapsulated in a solution of a stabilizer in an aliphatic hydrocarbon; b) preparing a solution of polyamine alone or optionally along with another polyamine in aliphatic hydrocarbon; c) adding solution prepared in step (b) drop wise to the dispersion of step (a) under agitation followed by treatment with anti-agglomerating agent to obtain microcapsules; and d) filtering and/or centrifuging, washing the microcapsules, with the aliphatic hydrocarbon and drying the microcapsules under vacuum at ambient temperature to obtain microcapsules with epoxy as capsule wall material.

7 . The process as claimed in claims 1 and 6 , wherein said stabilizer is selected from non-ionic polymeric surfactants having repeating hydrophilic and hydrophobic units, preferably polymeric non-ionic surfactant, more preferably Hydrophilic Lipophilic Balance (HLB) between 4 and 13.

8 . The process as claimed in claims 1 and 6 , wherein said epoxy component is selected from the group consisting of diglycidyl ether of bisphenol A, diglycidyl ethers of bisphenol F, epoxy phenol novolacs (EPN), epoxy cresol novolacs (ECN), diglycidyl ether of butane diol (Butyl dioldiglycidyl ether), 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexane carboxylate, triglycidyl-p-aminophenol, N,N,N,N-tetraglycidyl-4,4-methylenebis benzylamine, 4-glycidyloxy-N,N-di-glycidyl aniline, 1.1.2.2-(p-hydroxyphenol) ethane based epoxy resin, ethylene glycol diglycidyl ether, diethylene glycol diglycidyl ether, polyethyleneglycol diglycidyl ether, propylene glycol diglycidyl ether and glycerol polyglycidyl ether.

9 . The process as claimed in claim 6 , wherein said polyamine is selected from the group consisting of polyfunctional Aziridine PZ-33, PZ-28 (from Poly Aziridine L.L.C. NJ, USA), diethylenetriamine (DETA), triethylenetetraamine (TETA), tetraethylenepentamine, 2,4,4′-triaminodiphenylether, bis(hexamethylene) triamine, 1,4,5,8-tetraamino anthraquinone, ethylene diamine (EDA), trimethylenedipiperidine (TMDP), guanidine carbonate (GUCA), phenylenediamine, toluene diamine, pentamethylene hexamine, 1,6-hexamethylene diamine, 2,4-diamino-6-methyl-1,3,5 triazine 1,2-diaminocyclohexane, 4,4′-diamino diphenylmethane, 1,5-diaminonaphthalene-isophoronediamine, diamino propane, diaminobutane and mixtures thereof.

10 . The process as claimed in claims 1 and 6 , wherein said non-aqueous continuous medium for microencapsulation used as continuous phase may be selected from aliphatic hydrocarbon of the general formula C n H 2n+2 where n can be between 6 to 16 and is selected from hexane, octane, decane, isooctane, dodecane, hexadecane, superior kerosene, paraffin oil, white mineral oil or suitable mixtures thereof.

Assignees

• Council Scient Ind Res

Inventors

• Shukla Parshuram Gajanan
• Jadhav Arun Savalaram

Classifications

• C09J9/00

  Adhesives characterised by their physical nature or the effects produced, e.g. glue sticks (C09J7/00 takes precedence) · CPC title

• C09J2475/00

  Presence of polyurethane · CPC title

• C09J2205/11

  Chemistry & Metallurgy · mapped topic

• C09J163/00

  Adhesives based on epoxy resins; Adhesives based on derivatives of epoxy resins · CPC title

• C09J2463/00

  Presence of epoxy resin · CPC title