Process for preparing a thermo-expandable microspheres

• US 4,287,308 A
• Filed: 06/10/1980
• Issued: 09/01/1981
• Est. Priority Date: 02/14/1980
• Status: Expired due to Term

• Current Assignee: Matsumoto Yushi-Seiyaku Co., Ltd.
• Original Assignee: Matsumoto Yushi-Seiyaku Co., Ltd.
• Inventors: Kida, Sueo, Nakayama, Nobukazu
• Primary Examiner(s): Foelak, Morton
• Application Number:
  US06/158,172
• Time in Patent Office: 448 Days
• Field of Search: 521/53, 521/56, 521/149
• US Class Current: 521/53
• CPC Class Codes: C08J 9/16 Making expandable particles

Abstract

Microspheres, the blowing agent of which is microencapsulated with a thermoplastics having an acrylonitrile moiety, are prepared. Acrylonitrile monomer remaining therein is eliminated from the microspheres by cyanoethylation. The microspheres have an excellent solvent-resistance and an expansibility hardly changeable with time but no harmfulness attributed to the acrylonitrile monomer.

Claims

1. A process for preparing a thermo-expandable microsphere substantially free of acrylonitrile monomer which comprises microencapsulating a blowing agent with a thermoplastic polymer having an acrylonitrile moiety as one of ingredients, wherein the blowing agent becomes gaseous below a softening temperature of the thermoplastic polymer, and subjecting the microencapsulated product to cyanoethylation to eliminate the acrylonitrile monomer remaining in the microencapsulated product.

2. The process according to claim 1, wherein the thermoplastic polymer contains at least 15 percent by weight of the acrylonitrile moiety.

3. The process according to claim 1, wherein the thermoplastic polymer contains at least 15 percent by weight of the acrylonitrile moiety, 30 to 80 percent by weight of a vinylidene chloride moiety and 0.1 to 1.0 percent by weight of a cross-linkable vinyl monomer moiety.

4. The process according to claim 1, wherein the cyanoethylation is carried out at 30°

to 80°

C. under 2 to 10 Kg/cm².

5. The process according to claim 1, wherein the cyanoethylation is effected using a compound selected from the group consisting of primary amine, secondary amine, primary alkanolamine, secondary alkanolamine, secondary alkylalkanolamine and sodium sulfide.