The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Jan. 11, 1994

Filed:

Jan. 21, 1992
Applicant:
Inventors:

Rolf Mulhaupt, Marly, CH;

Jeremy H Powell, Horseheath, GB;

Christopher S Adderley, Hardwick, GB;

Werner Rufenacht, Marly, CH;

Assignee:

Ciba-Geigy Corporation, Ardsley, NY (US);

Attorneys:
Primary Examiner:
Int. Cl.
CPC ...
C08L / ; C08L / ; C08L / ; C08L / ;
U.S. Cl.
CPC ...
525454 ; 525 65 ; 525 66 ; 525 68 ; 525 92 ; 525 93 ; 525 94 ; 525107 ; 525109 ; 525127 ; 525128 ; 525129 ; 525130 ; 525131 ; 525146 ; 525147 ; 525148 ; 525150 ; 525151 ; 525423 ; 525424 ; 525426 ; 525438 ; 525439 ; 525440 ; 525445 ; 525450 ; 525453 ; 525528 ;
Abstract

Compositions containing A) a copolymer based on at least one 1,3-diene and at least one polar, ethylenically unsaturated comonomer and B) a phenol-terminated polyurethane, polyurea or polyurea-urethane of the formula I ##STR1## in which m is 1 or 2, n is 2 to 6, R.sup.1 is the n-valent radical of an elastomeric prepolymer which is soluble or dispersible in epoxide resins, X and Y independently of one another are --O-- or --NR.sup.3 --, it being necessary for one of these groups to be --NR.sup.3 --, R.sup.2 is an m+1-valent radical of a polyphenol or aminophenol after the removal of the phenolic hydroxy group(s) or the amino group or both the amino group and the phenolic hydroxyl group, respectively, and R.sup.3 is hydrogen, C.sub.1 -C.sub.6 alkyl or phenyl, are described. Compounds containing the components A) and B) as well as an epoxide resin C) are also described. The cured products are distinguished by a high peel strength and high resistance to crack propagation. The curable compositions can be employed, for example, as structural adhesives.


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