IP Library Granted Patent US 7,297,804
Granted Patent B2
US 7,297,804 · App. 10/536,658 · Granted Nov 20, 2007

Catalytic composition of organotin compounds

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Quick Facts
Patent No.
US 7,297,804
App. No.
10/536,658
Granted
Nov 20, 2007
Kind
B2
Abstract

The present invention relates to catalytic compositions for esterification, transestrification and polycondensation reactions, a process for the catalysis of said reactions employing such catalytic compositions and polyesters for resins obtainable by this process.

Claims (28)

1. A catalytic composition for esterification, transesterification and polycondensation reactions of dicarboxylic acids, polycarboxylic acids and/or hydroxy carboxylic acids and alcohols, said catalytic composition containing a tin compound of the general formula (I):

[(R 1 Sn) l (OH) m-n (OR 2 ) n O o ] p+ A q− p/q   (formula I)

wherein:

R 1 and R 2 each independently is a linear, branched or cyclic alkyl group or aryl group having 1 to 12 carbon atoms,

A q− is an anion,

l=12,

m=6,

n=1 to 6,

o=14,

p=2 and

q=1 to 2.

2. The catalytic composition according to claim 1 , wherein the anion A q− is O 2− , OH − , a linear, branched or cyclic alkyl carboxy group, aryl carboxy group or alkoxy group each having 1 to 12 carbon atoms, the anion of a mineral acid or a metalate.

3. The catalytic composition according to claim 2 , wherein the anion A q− is a sulphate, sulphite, phosphate, halogenide or pseudo-halogenide, titanate, zirconate, aluminate or zincate anion.

4. The catalytic composition according to claim 1 , wherein the anion A q− is a chloride anion and R 1 is an octyl- and/or butyl group.

5. A process for the preparation of a catalytic composition according to claim 1 , said process comprising the step of reacting a metal alkoxide with a tin compound of the general formula:

[(R 1 Sn) l (OH) m O o ] P+ A q− p/q·

6. The process according to claim 5 , wherein said metal alkoxide and said tin compound are reacted in a mole proportion of 1:0.0001 up to 1:20, in particular 1:4 to 1:6, respectively.

7. The process according to claim 6 , wherein resultant metal oxides, metal hydroxides and/or alkoxy metal hydroxides remain in the catalytic composition.

8. The process according to claim 5 , wherein resultant metal oxides, metal hydroxides and/or alkoxy metal hydroxides remain in the catalytic composition.

9. A method for the continuous or batchwise production of esters or polycondensation products by esterification, transesterification, polyesterification or polytransesterification reaction, said method comprising using the catalytic composition as defined in claim 1 .

10. The method according to claim 9 , comprising a polyesterification reaction of a dicarboxylic acid derivative with a mono, divalent or polyvalent alcohol in the presence of the catalytic composition.

11. The method according to claim 10 , employing derivatives of di or polycarboxylic acids selected from the group of esters or halogenides.

12. The method according to claim 9 , employing derivatives of di or polycarboxylic acids selected from the group of esters or halogenides.

13. The method according to claim 9 , employing derivatives of hydroxycarboxylic acids selected from esters.

14. The method according to claim 9 , employing a metal concentration of said catalytic composition in the range of 0.1 ppm to 1 mole percent, in particular 10-100 ppm with reference to the acid or derivative to be reacted.

15. The method according to claim 9 , employing a solvent or suspending agent for the manufacturing of the catalytic composition and/or said esterification, transesterification, polyesterification or polytransesterification reaction.

16. The method according to claim 15 , employing the same solvent and/or suspending agent in the manufacturing of said catalytic composition and said esterification, transesterification, polyesterification or polytransesterification reaction.

17. The method according to claim 15 , employing a solvent or suspending agent selected from the group consisting of mono-, di- or polyvalent alcohols being reacted in said esterification, transesterification, polyesterification or polytransesterification reaction.

Assignments (2)
CHANGE OF NAME Recorded Nov 3, 2006
From: CROMPTON GMBH
To: CHEMTURA ORGANOMETALLICS GMBH
Reel/Frame 018490/0304 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 27, 2005
From: RODER, JENS; KAPRIES, ADREA; FRANKE, LIANE; SCHUMACHER, OLIVER; CANISIUS, JOHANNES
To: CROMPTON GMBH
Reel/Frame 017102/0254 →