IP Library Granted Patent US 7,235,601
Granted Patent B2
US 7,235,601 · App. 10/684,601 · Granted Jun 26, 2007

Hydrogenated nitrile rubber compositions with improved processability

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Quick Facts
Patent No.
US 7,235,601
App. No.
10/684,601
Granted
Jun 26, 2007
Kind
B2
Abstract

The present invention relates to polymer composites containing at least one, optionally hydrogenated, nitrile rubber polymer having a Mooney viscosity (ML 1+4 @ 100° C.) in the range of from 50–30 at least one filler and optionally at least one cross-linking agent, a process for preparing said polymer composite wherein at least one, optionally hydrogenated, nitrile rubber polymer having a Mooney viscosity (ML 1+4 @ 100° C.) in the range of from 50–30, at least one filler and optionally at least one cross-linking agent are mixed and a process for the manufacture of a shaped article including the step of injection molding a polymer composite containing at least one, optionally hydrogenated, nitrile rubber polymer having a Mooney viscosity (ML 1+4 @ 100° C.) in the range of from 50-30, at least one filler and at least one cross-linking agent.

Claims (29)

1. A polymer composite consisting of at least one, optionally hydrogenated, nitrile rubber polymer having a Mooney viscosity (ML 1+4 @ 100° C.) in the range of from 50–30 and a polydispersity index of less than 2.7, at least one filler and optionally at least one cross-linking agent,

wherein the optionally hydrogenated, nitrile rubber polymer is prepared by a metathesis reaction in the presence of one or more compounds of the general formulas I, II, III or IV

 wherein:

M is Os or Ru,

R and R 1 are, independently, hydrogen or a hydrocarbon selected from the group consisting of C 2 –C 20 alkenyl, C 2 –C 20 alkynyl, C 1 –C 20 alkyl, aryl, C 1 –C 20 carboxylate, C 1 –C 20 alkoxy, C 2 –C 20 alkenyloxy, C 2 –C 20 alkynyloxy, aryloxy, C 2 –C 20 alkoxycarbonyl, C 1 –C 20 alkylthio, C 1 –C 20 alkylsulfonyl and C 1 –C 20 alkylsulfinyl,

X and X 1 are independently any anionic ligand, and

L and L 1 are independently any neutral ligand or any neutral carbene, optionally, L and L 1 can be linked to one another to from a bidentate neutral ligand;

 wherein:

M 1 is Os or Ru;

R 2 and R 3 are, independently, hydrogen or a hydrocarbon selected from the group consisting of C 2 –C 20 alkenyl, C 2 –C 20 alkynyl, C 1 –C 20 alkyl, aryl, C 1 –C 20 carboxylate, C 1 –C 20 alkoxy, C 2 –C 20 alkenyloxy, C 2 –C 20 alkynyloxy, aryloxy 2 –C 20 alkoxycarbonyl, C 1 –C 20 alkylthio, C 1 –C 20 alkylsulfonyl and C 1 –C 20 alkylsulfinyl,

X 2 is anionic ligand, and

L 2 is a neutral π-bonded ligand, independent of whether is mono- or polycyclic,

L 3 is a ligand selected from the group consisting of phosphines, sulfonated phosphines, fluorinated phosphines, functionalized phosphines bearing up to three aminoalkyl-, ammoniumalkyl-, alkoxyalkyl-, alkoxylcarbonylalkyl-, hydrocycarbonylalkyl-, hydroxyalkyl- or ketoalkyl- groups, phosphites, phosphinites, phosphonites, phophinamines, arsines, stibenes, ethers, amines, amides, imines, sulfoxides, thioethers and pyridines, Y- is a non-coordinating anion, n is an integer in the range of from 0 to 5;

 wherein

M 2 is Mo or W,

R 4 and R 5 are, independently, hydrogen or a hydrocarbon selected from the group consisting of C 2 –C 20 alkenyl, C 2 –C 20 alkynyl, C 1 –C 20 alkyl,

 aryl, C 1 –C 20 carboxylate, C 1 –C 20 alkoxy, C 2 –C 20 alkenyloxy, C 2 –C 20 alkynyloxy, aryloxy, C 2 –C 20 alkoxycarbonyl, C 1 –C 20 alkyrlthio, C 1 –C 20 alkylsulfonyl and C 1 –C 20 alkylsulfinyl,

R 6 and R 7 are independently selected from any unsubstituted or halo-substituted alkyl, aryl, aralkyl groups or silicon-containing analogs thereof:

 wherein:

M is Os or Ru,

R and R 1 are independently selected from the group consisting of hydrogen, substituted or unsubstituted alkyl, and substituted or unsubstituted alkyl,

X and X 1 are independently any anionic ligand, and

L and L 1 are independently any neutral ligand, or any neutral carbene, optionally, L and L 1 can be linked to one another to form a bidentate neutral ligand.

2. The polymer composite according to claim 1 wherein the Mooney viscosity (ML 1+4 @ 100° C.) is in the range of from 45–30.

3. The polymer composite according to claim 1 wherein the Mooney viscosity (ML 1+4 @ 100° C.) is in the range of from 40–30.

4. The polymer composite according to claim 1 , wherein the optional cross-lining agent is selected peroxide or sulfur curing system.

5. A process for preparing the polymer composite according claim 1 comprising mixing the least one, optionally hydrogenated, nitrile rubber polymer having a Mooney viscosity (ML 1+4 @ 100° C.) in the range of from 50–30 and a polydispersity index of less than 2.7, the at least one filler and optionally the at least one cross-linking agent.

6. A process for the manufacture of a shaped article comprising the step of injection molding a polymer composite according to claim 1 .

7. The process according to claim 6 , wherein the shaped article is a seal, a hose, a beating pad, a stator, a well head seal, a valve plate, a cable sheathing, a wheel roller, a belt, in place gaskets or a pipe seal.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 18, 2006
From: BAYER INC.
To: LANXESS INC.
Reel/Frame 017186/0200 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 30, 2004
From: GUERIN, FREDERIC; FERRARI, LORENZO; GAMLIN, JANET; PAZUR, RICHARD; VON HELLENS, CARL WALTER; CAMPOMIZZI, EZIO C.
To: BAYER INC.
Reel/Frame 014931/0960 →