IP Library Granted Patent US 7,799,891
Granted Patent B2
US 7,799,891 · App. 12/611,380 · Granted Sep 21, 2010

Phosphorus containing compounds for reducing acetaldehyde in polyesters polymers

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Quick Facts
Patent No.
US 7,799,891
App. No.
12/611,380
Granted
Sep 21, 2010
Kind
B2
Abstract

Polyesters whose polycondensation is catalyzed by titanium-containing catalysts and which are susceptible to acetaldehyde formation during polycondensation or subsequent molding operations are prepared with low finished acetaldehyde content and reduced acetaldehyde generation by adding an ammonium or amine salt of an oxyphosphorus-acid. Polyesters, especially polyethylene terephthalate, may be produced with high inherent viscosity in reduced processing time, without the necessity of further polymerization in the solid state.

Claims (18)

1. A method of forming a bottle preform, comprising:

(i) introducing into a melt processing zone a stream comprising an amine salt of one or more of phosphorous acid and phosphoric acid and a stream comprising solid polyester particles having a residual acetaldehyde level of 10 ppm or less, wherein the polyester is formed from terephthalic acid and ethylene glycol, and the polyester is modified with one or more modifiers in an amount less than 15 mole %;

(ii) melting the particles to form a molten polyester polymer composition; and

(iii) forming a bottle preform from the molten polymer composition.

2. The method of claim 1 , wherein the bottle preform has a residual acetaldehyde content of 10 ppm or less.

3. The method of claim 1 , wherein the bottle preform has a residual acetaldehyde content of 8 ppm or less.

4. A method comprising

(i) introducing into a melt processing zone:

(a) a stream of polyester particles containing a randomly dispersed amine salt of one or more of phosphorous acid and phosphoric acid, and

(b) a stream comprising solid polyester particles having a residual acetaldehyde level of 10 ppm or less, wherein the solid polyester particles comprise a polyester formed from terephthalic acid and ethylene glycol that is modified with one or more modifiers in an amount less than 15 mole %;

(ii) melting the particles to form a molten polyester polymer composition; and

(iii) forming a bottle preform from the molten polymer composition.

5. The method of claim 4 , wherein the bottle preform has a residual acetaldehyde content of 10 ppm or less.

6. The method of claim 4 , wherein the bottle preform has a residual acetaldehyde content of 8 ppm or less.

7. The method of claim 1 , wherein the one or more modifiers comprise one or more of phthalic acid, isophthalic acid, naphthalene-2,6-dicarboxylic acid, 1,4-cyclohexanedicarboxylic acid, 1,3-cyclohexanedicarboxylic acid, diethylene glycol, triethylene glycol, 1,4-cyclohexanedimethanol, propane-1,2-diol, propane-1,3-diol, butane-1,4-diol, pentane-1,5-diol, hexane-1,6-diol, 3-methylpentane-2,4-diol, 2-methylpentane-1,4-diol, 2,2,4-trimethylpentane-1,3-diol, 2-ethylhexane-1,3-diol, 2,2-diethylpropane-1,3-diol, hexane-1,3-diol, 1,4-di(hydroxyethoxy)-benzene, 2,2-bis-(4-hydroxycyclohexyl)-propane, 2,4-dihydroxy-1,1,3,3-tetramethylcyclobutane, 2,2-bis-(3-hydroxyethoxyphenyl)-propane, 2,2-bis-(4-hydroxypropoxyphenyl)-propane, 1,2-cyclohexanediol, or 1,4-cyclohexanediol.

8. The method of claim 1 , wherein the one or more modifiers comprise one or more of isophthalic acid, 1,4-cyclohexanedicarboxylic acid, diethylene glycol, triethylene glycol, 1,4-cyclohexanedimethanol, butane-1,4-diol, or 2,4-dihydroxy-1,1,3,3-tetramethylcyclobutane, 1,2-cyclohexanediol, or 1,4-cyclohexanediol.

9. The method of claim 4 , wherein the one or more modifiers comprise one or more of phthalic acid, isophthalic acid, naphthalene-2,6-dicarboxylic acid, 1,4-cyclohexanedicarboxylic acid, 1,3-cyclohexanedicarboxylic acid, diethylene glycol, triethylene glycol, 1,4-cyclohexanedimethanol, propane-1,2-diol, propane-1,3-diol, butane-1,4-diol, pentane-1,5-diol, hexane-1,6-diol, 3-methylpentane-2,4-diol, 2-methylpentane-1,4-diol, 2,2,4-trimethylpentane-1,3-diol, 2-ethylhexane-1,3-diol, 2,2-diethylpropane-1,3-diol, hexane-1,3-diol, 1,4-di(hydroxyethoxy)-benzene, 2,2-bis-(4-hydroxycyclohexyl)-propane, 2,4-dihydroxy-1,1,3,3-tetramethylcyclobutane, 2,2-bis-(3-hydroxyethoxyphenyl)-propane, 2,2-bis-(4-hydroxypropoxyphenyl)-propane, 1,2-cyclohexanediol, or 1,4-cyclohexanediol.

10. The method of claim 4 , wherein the one or more modifiers comprise one or more of isophthalic acid, 1,4-cyclohexanedicarboxylic acid, diethylene glycol, triethylene glycol, 1,4-cyclohexanedimethanol, butane-1,4-diol, or 2,4-dihydroxy-1,1,3,3-tetramethylcyclobutane, 1,2-cyclohexanediol, or 1,4-cyclohexanediol.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 1, 2011
From: EASTMAN CHEMICAL COMPANY
To: GRUPO PETROTEMEX, S.A. DE C.V.
Reel/Frame 025727/0271 →