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US5120475A Expired / Lapsed US ⏱️ 0.0 years remaining

Method for preparing microcapsules having improved pre-walls, and microcapsules and photosensitive materials produced thereby

Assignee: Cycolor Imaging Inc
•
Filing: 1990-04-19
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Granted: 1992-06-09
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Expires: 2010-04-19
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Abstract

Abstract A method for preparing microcapsules which comprises: dispersing a hydrophobic oily liquid containing a pre-wall former in a continuous aqueous phase, the aqueous phase containing a chain extender which comprises a water soluble polyfunctional compound capable of reacting with the pre-wall former upon dispersion of the hydrophobic oily liquid in the continuous aqueous phase; and forming capsule walls around the droplets of the hydrophobic oily liquid in the continuous aqueous phase.

Inventors

  • 👤 Jing-Den Chen
  • 👤 Kerry Kovacs
  • 👤 M. Teresa Thomas
  • 👤 Rong-Chang Liang

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-27 18:41
CPC Classifications
G; G03; G03F; G03F7/00; G03F7/002; G03F7/0022; B; B01; B01J; B01J13/00; B01J13/02; B01J13/06; B01J13/14; B01J13/16; B01J13/20; B01J13/22; Y; Y10; Y10T; Y10T428/00; Y10T428/249921; Y10T428/249994; Y10T428/249995; Y10T428/249997

Claims Analysis

Total Claims: 24
Claim 1
Independent Claim 167 words
A method for preparing microcapsules which comprises: dispersing a hydrophobic oily liquid containing a pre-wall former in a continuous aqueous phase, wherein said pre-wall former is selected from the group consisting of a polyvalent isocyanate, a polyvalent isothiocyanate, a polyvalent isocyanate adduct, a polyvalent isothiocyanate adduct, a cyanoacrylate, an isocyanato acrylate, and a mixture of a polyvalent isocyanate and a sulfonated polyvalent isocyanate, said aqueous phase containing at least one water soluble chain extender which also has a high affinity toward said oily liquid, said chain extender selected from the group consisting of melamine, methylol derivatives of melamine, ethylenediamine, diethylenetriamine, triethylenetetraamine, sorbitol, glycerine, N,N,N',N'-tetrakis (2-hydroxyethyl) ethylenediamine, lysine, glutamine, glactosamine, 2-amino-2-ethyl-1,3-propanediol, 2-(2-amino-ethylamino) ethanol, 1-(aminoethyl)-4-hydroxybenzyl alcohol, and 1,3-diamino-2-hydroxy propane wherein said chain extender reacts with said pre-wall former upon dispersion of said hydrophobic oily liquid in said continuous aqueous phase to form a thick, non-permeable pre-wall surrounding the oil droplets; and forming capsule walls around the pre-wall coated droplets of said hydrophobic oily liquid in said continuous aqueous phase.
Claim 2
Independent Claim 167 words
A method for preparing microcapsules which comprises: dispersing a hydrophobic oily liquid containing a pre-wall former in a continuous aqueous phase, wherein said pre-wall former is selected from the group consisting of a polyvalent isocyanate, a polyvalent isothiocyanate, a polyvalent isocyanate adduct, a polyvalent isothiocyanate adduct, a cyanoacrylate, an isocyanato acrylate, and a mixture of a polyvalent isocyanate and a sulfonated polyvalent isocyanate, said aqueous phase containing at least one water soluble chain extender which also has a high affinity toward said oily liquid, said chain extender selected from the group consisting of melamine, methylol derivatives of melamine, ethylenediamine, diethylenetriamine, triethylenetetraamine, sorbitol, glycerine, N,N,N',N'-tetrakis (2-hydroxyethyl) ethylenediamine, lysine, glutamine, glactosamine, 2-amino-2-ethyl-1,3-propanediol, 2-(2-amino-ethylamino) ethanol, 1-(aminoethyl)-4-hydroxybenzyl alcohol, and 1,3-diamino-2-hydroxy propane wherein said chain extender reacts with said pre-wall former upon dispersion of said hydrophobic oily liquid in said continuous aqueous phase to form a thick, non-permeable pre-wall surrounding the oil droplets; and forming capsule walls around the pre-wall coated droplets of said hydrophobic oily liquid in said continuous aqueous phase.
Claim 3
Dependent Claim 24 words
The method of claim 1 wherein said chain extender is selected from the group consisting of melamine, ethylenediamine, diethylenetriamine, triethylenetetraamine, sorbitol, glycerol and lysine.
Claim 4
Dependent Claim 13 words
The method of claim 2 wherein said chain extender is melamine, or sorbitol.
Claim 5
Dependent Claim 19 words
The method of claim 3 wherein said microcapsule walls are formed by forming in situ an amine-formaldehyde condensation product.
Claim 6
Dependent Claim 14 words
The method of claim 4 wherein said condensation product is a melamine-formaldehyde condensation product.
Claim 7
Dependent Claim 25 words
The method of claim 1 wherein said pre-wall former is a polyvalent isocyanate or a mixture of a polyvalent isocyanate and a sulfonated polyvalent isocyanate.
Claim 8
Dependent Claim 21 words
The method of claim 6 wherein said pre-wall former is a mixture of a polyvalent isocyanate and a sulfonated polyvalent isocyanate.
Claim 9
Dependent Claim 18 words
The method of claim 1 wherein said continuous aqueous phase contains a water soluble anionic polymer dissolved therein.
Claim 10
Dependent Claim 22 words
The method of claim 8 wherein said water soluble anionic polymer is a homopolymer or a copolymer of vinyl benzene sulfonic acid.
Claim 11
Dependent Claim 14 words
The method of claim 1 wherein said hydrophobic oily liquid is a photohardenable composition.
Claim 12
Dependent Claim 20 words
The method of claim 1 wherein said continuous aqueous phase further contains an anionic, cationic, or nonionic surface active agent.
Claim 13
Dependent Claim 14 words
The method of claim 11 wherein said surface active agent is a sulfonated polystyrene.
Claim 14
Independent Claim 189 words
A method for forming melamine-formaldehyde microcapsules which comprises: dispersing a hydrophobic oily liquid containing a pre-wall former in a continuous aqueous phase to form a dispersion, wherein said pre-wall former is selected from the group consisting of a polyvalent isocyanate, a polyvalent isothiocyanate, a polyvalent isocyanate adduct, a polyvalent isothiocyanate adduct, a cyanoacrylate, an isocyanato acrylate, and a mixture of a polyvalent isocyanate and a sulfonated polyvalent isocyanate, said aqueous phase containing at least one water soluble chain extender which also has a high affinity toward said oily liquid, said chain extender selected from the group consisting of melamine, methylol derivatives of melamine, ethylenediamine, diethylenetriamine, triethylenetetraamine, sorbitol, glycerine, N,N,N',N'-tetrakis (2-hydroxyethyl) ethylenediamine, lysine, glutamine, glactosamine, 2-amino-2-ethyl-1,3-propanediol, 2-)2-amino-ethylamino) ethanol, 1-(aminoethyl)-4-hyeroxybenzyl alcohol, 1,3-diamino-2-hydroxy propane wherein said chain extender reacts with said pre-wall former upon dispersion of said hydrophobic oily liquid in said continuous aqueous phase to form a thick, non-permeable pre-wall surrounding the oil droplets; and adding aqueous solutions of melamine and formaldehyde or an aqueous solution of a prepolymer thereof to said dispersion to form a melamine-formaldehyde condensate which enwraps the pre-wall coated oily particles forming said dispersion to form microcapsules.
Claim 15
Independent Claim 189 words
A method for forming melamine-formaldehyde microcapsules which comprises: dispersing a hydrophobic oily liquid containing a pre-wall former in a continuous aqueous phase to form a dispersion, wherein said pre-wall former is selected from the group consisting of a polyvalent isocyanate, a polyvalent isothiocyanate, a polyvalent isocyanate adduct, a polyvalent isothiocyanate adduct, a cyanoacrylate, an isocyanato acrylate, and a mixture of a polyvalent isocyanate and a sulfonated polyvalent isocyanate, said aqueous phase containing at least one water soluble chain extender which also has a high affinity toward said oily liquid, said chain extender selected from the group consisting of melamine, methylol derivatives of melamine, ethylenediamine, diethylenetriamine, triethylenetetraamine, sorbitol, glycerine, N,N,N',N'-tetrakis (2-hydroxyethyl) ethylenediamine, lysine, glutamine, glactosamine, 2-amino-2-ethyl-1,3-propanediol, 2-)2-amino-ethylamino) ethanol, 1-(aminoethyl)-4-hyeroxybenzyl alcohol, 1,3-diamino-2-hydroxy propane wherein said chain extender reacts with said pre-wall former upon dispersion of said hydrophobic oily liquid in said continuous aqueous phase to form a thick, non-permeable pre-wall surrounding the oil droplets; and adding aqueous solutions of melamine and formaldehyde or an aqueous solution of a prepolymer thereof to said dispersion to form a melamine-formaldehyde condensate which enwraps the pre-wall coated oily particles forming said dispersion to form microcapsules.
Claim 16
Dependent Claim 24 words
The method of claim 13 wherein said chain extender is selected from the group consisting of melamine, sorbitol, glycerol, ethylenediamine, diethylenetriamine, triethylenetetraamine, and lysine.
Claim 17
Dependent Claim 13 words
The method of claim 14 wherein said chain extender is melamine or sorbitol.
Claim 18
Dependent Claim 23 words
The method of claim 1 wherein said pre-wall former is a polyisocyanate or a mixture of a polyisocyanate and a sulfonated polyvalent isocyanate.
Claim 19
Dependent Claim 19 words
The method of claim 16 wherein said pre-wall former is a mixture of a polyisocyanate and a sulfonated polyisocyanate.
Claim 20
Dependent Claim 18 words
The method of claim 13 wherein said continuous aqueous phase contains a water soluble anionic polymer dissolved therein.
Claim 21
Dependent Claim 22 words
The method of claim 18 wherein said water soluble anionic polymer is a homopolymer or a copolymer of vinyl benzene sulfonic acid.
Claim 22
Dependent Claim 14 words
The method of claim 13 wherein said hydrophobic oily liquid is a photohardenable composition.
Claim 23
Dependent Claim 20 words
The method of claim 13 wherein said continuous aqueous phase further contains an anionic, cationic, or nonionic surface active agent.
Claim 24
Dependent Claim 14 words
The method of claim 21 wherein said surface active agent is a sulfonated polystyrene.

References Cited (Backward Citations)

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US4608330A Cited
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USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1995-06-09 1995-12-09 1996-06-09 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1999-06-09 1999-12-09 2000-06-09 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2003-06-09 2003-12-09 2004-06-09 $7700.00 Window Closed / Lapsed

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