Sulfonated aromatic copolyesters containing hydroxyalkanoic acid groups and shaped articles produced therefrom

a technology of aromatic copolyesters and hydroxyalkanoic acid, which is applied in the direction of packaging, fastening means, synthetic resin layered products, etc., can solve the problems of insufficient low temperature impact strength of pet sheets, etc., to achieve optimized balance of physical properties, deadfold performance, toughness, thermal dimensional stability, etc.

Inactive Publication Date: 2006-01-12
EI DU PONT DE NEMOURS & CO
View PDF14 Cites 21 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

This patent describes various methods for producing improved materials with specific chemical characteristics that are suitable for use in applications like food packaging. These materials include sulfoacid ester compounds made by reacting certain types of fatty acids together with another type of alcohol at different temperatures. Sulfurized polymers obtained through these techniques provide excellent mechanical strength, heat resistance, and moisture barriers compared to existing coatings used on plastics. Additionally, they also improve compatibility with other components during production and processing conditions.

Problems solved by technology

This patent describes various methods for improving the performance of thermoplastic resins used in packaging products. These techniques involve adding specific chemical groups to these resins to improve their thermal properties. Examples include introducing sulfur atoms onto the molecules themselves, attaching esters on the backbone of the resins, modifying the structure of the resins through chemical reactions, incorporating sulfonate functions, and introducing sulfoacid moieties into the structures. Additionally, it suggests using sulfonated aliphatic-arachoic copolymers containing hydroxy alkanoic acids instead of hydroxypropyl monocarboxylic acid.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Examples

Experimental program
Comparison scheme
Effect test

examples

Test Methods.

[0179] Differential Scanning Calorimetry, (DSC), is performed on a TA Instruments Model Number 2920 machine. Samples are heated under a nitrogen atmosphere at a rate of 20 degrees C. / minute to 300 degrees C., programmed cooled back to room temperature at a rate of 20 degrees C. / minute and then reheated to 300 degrees C. at a rate of 20 degrees C. / minute. The observed sample glass transition temperature, (Tg), and crystalline melting temperature, (Tm), noted below were from the second heat.

[0180] Inherent Viscosity, (IV), is defined in “Preparative Methods of Polymer Chemistry”, W. R. Sorenson and T. W. Campbell, 1961, p. 35. It is determined at a concentration of 0.5 g. / 100 mL of a 50:50 weight percent trifluoroacetic acid:dichloromethane acid solvent system at room temperature by a Goodyear R-103B method.

[0181] Laboratory Relative Viscosity, (LRV), is the ratio of the viscosity of a solution of 0.6 gram of the polyester sample dissolved in 10 mL of hexafluoroi

example 1

[0185] To a 250 milliliter glass flask was added bis(2-hydroxyethyl)terephthalate, (150.26 grams), glycolic acid, (17.66 grams), dimethyl 5-sulfoisophthalate, sodium salt, (2.66 grams), sodium acetate, (0.19 grams), manganese(II) acetate tetrahydrate, (0.0584 grams), and antimony(III) trioxide, (0.0470 grams). The reaction mixture was stirred and heated to 180 C under a slow nitrogen purge. After achieving 180 C, the reaction mixture was stirred at 180 C for 0.6 hours under a slow nitrogen purge. The reaction mixture was then heated to 240 C over 0.6 hours with stirring. After achieving 240 C, the reaction mixture was stirred at 240 C for 0.5 hours under a slow nitrogen purge. The reaction mixture was then heated to 255 C over 0.1 hours with stirring under a slight nitrogen purge. The reaction mixture was stirred at 255 C for 1.0 hour under a slight nitrogen purge. 8.2 grams of a colorless distillate was collected over this heating cycle. The reaction mixture was then staged to full va

example 2

[0188] 35 To a 250 milliliter glass flask was added bis(2-hydroxyethyl)terephthalate, (150.26 grams), poly(lactide), (12.90 grams), dimethyl 5-sulfoisophthalate, sodium salt, (2.67 grams), sodium acetate, (0.18 grams), manganese(II) acetate tetrahydrate, (0.0577 grams), and antimony(III) trioxide, (0.0466 grams). The reaction mixture was stirred and heated to 180 C under a slow nitrogen purge. After achieving 180 C, the reaction mixture was stirred at 180 C for 0.5 hours under a slow nitrogen purge. The reaction mixture was then heated to 240 C over 0.2 hours with stirring. After achieving 240 C, the reaction mixture was stirred at 240 C for 0.8 hours under a slow nitrogen purge. The reaction mixture was then heated to 255 C over 0.3 hours with stirring under a slight nitrogen purge. The reaction mixture was stirred at 255 C for 0.8 hours under a slight nitrogen purge. 3.7 grams of a colorless distillate was collected over this heating cycle. The reaction mixture was then staged to ful

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

PropertyMeasurementUnit
Fractionaaaaaaaaaa
Thicknessaaaaaaaaaa
Thicknessaaaaaaaaaa
Login to view more

Abstract

Sulfonated aromatic copolyesters and articles made therefrom, and processes for producing the sulfonated aromatic copolyesters and articles are provided. Articles that can be made from the sulfonated aromatic copolyesters include films, coatings and laminates. Some of the compositions and articles are biocompostable. The films can further be used to form shaped articles such as sheets, food packaging such as sandwich wraps, thermoformed containers, and coatings for, for example, films and other substrates. The sulfonated aromatic copolyesters contain a hydroxyalkanoic acid component.

Description

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Owner EI DU PONT DE NEMOURS & CO
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products