Unlock instant, AI-driven research and patent intelligence for your innovation.

Sulfonated aliphatic-aromatic polyetherester films, coatings, and laminates

A technology of sulfonated fat and copolyetherester, applied in the field of sulfonated aliphatic-aromatic polyetherester

Inactive Publication Date: 2010-05-26
EI DU PONT DE NEMOURS & CO
View PDF108 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the use of polymer blends may require additional and / or complex steps in the formation of films, coatings or laminates

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

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Sulfonated aliphatic-aromatic polyetherester films, coatings, and laminates

Examples

Experimental program
Comparison scheme
Effect test

preparation Embodiment PE1

[0194] Bis(2-hydroxyethyl)terephthalate (508.48 g), dimethyl glutarate (82.14 g), dimethyl 5-sulfoisophthalate sodium salt ( 15.19g), tris(2-hydroxyethyl) trimellitate (2.23g), polyethylene glycol (average molecular weight=1450, 42.38g), sodium acetate (0.76g), manganese (II) acetate Water (0.2363g) and antimony(III) trioxide (0.1902g). The reaction mixture was stirred and heated to 180°C under a slow nitrogen purge. After reaching 180 °C, the reaction mixture was heated to 200 °C within 0.2 h under a slow nitrogen purge and stirring. The obtained reaction mixture was stirred at 200 °C for 1 h under a slight nitrogen purge. Subsequently, the reaction mixture was heated to 275 °C within 1.3 h with stirring under a slight nitrogen purge. The obtained reaction mixture was stirred at 275° C. for 1.2 h under slight nitrogen blowing. During this heating cycle, 67.0 g of colorless distillate was collected. Subsequently, the reaction product entered a full vacuum stage and was st...

preparation Embodiment PE2

[0199] Into a 250 mL glass flask was added bis(2-hydroxyethyl) terephthalate (99.15 g), dimethyl glutarate (16.02 g), dimethyl 5-sulfoisophthalate sodium salt (2.96 g), polyethylene glycol (average molecular weight = 1000) (8.14 g), manganese (II) acetate tetrahydrate (0.042 g) and antimony (III) trioxide (0.034 g). The reaction mixture was stirred and heated to 180°C under a slow nitrogen purge. After reaching 180 °C, the reaction mixture was heated to 200 °C within 0.4 h under a slow nitrogen purge and stirring. The obtained reaction mixture was stirred at 200 °C for 1.1 h under a slight nitrogen blow. Subsequently, the reaction mixture was heated to 275 °C within 1.6 h with stirring under a slight nitrogen purge. The obtained reaction mixture was stirred at 275° C. for 1.2 h under slight nitrogen blowing. During this heating cycle, 9.67 g of colorless distillate was collected. Subsequently, the reaction product entered a full vacuum stage and was stirred at 275°C. The ...

preparation Embodiment PE3

[0203] Into a 250 mL glass flask was added bis(2-hydroxyethyl) terephthalate (99.15 g), dimethyl glutarate (16.02 g), dimethyl 5-sulfoisophthalate sodium salt (2.96 g), polyethylene glycol (average molecular weight = 2000) (8.14 g), manganese (II) acetate tetrahydrate (0.042 g) and antimony (III) trioxide (0.034 g). The reaction mixture was stirred and heated to 180°C under a slow nitrogen purge. After reaching 180 °C, the reaction mixture was heated to 200 °C within 0.3 h under a slow nitrogen purge and stirring. The obtained reaction mixture was stirred at 200 °C for 1.1 h under a slight nitrogen blow. Subsequently, the reaction mixture was heated to 275 °C within 1.3 h under a slow nitrogen purge. The obtained reaction mixture was stirred at 275 °C for 1.0 h under a slight nitrogen blow. During this heating cycle, 7.60 g of colorless distillate was collected. Subsequently, the reaction product entered a full vacuum stage and was stirred at 275°C. The resulting reaction...

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
diameteraaaaaaaaaa
diameteraaaaaaaaaa
particle sizeaaaaaaaaaa
Login to View More

Abstract

Articles, including films, coatings and laminates, are produced from certain sulfonated aliphatic-aromatic polyetherester compositions, which have an optimized combination of fast biodegradation ratesand enhanced thermal properties when compared to the sulfonated aliphatic-aromatic polyetherester compositions of the art. The articles may be further processed to form useful shaped articles, such as sheets, thermoformed containers, and coatings that can be applied to, for example, films or other substrates. The disclosed polyetheresters are based on copolyesters produced from a mixture containing aromatic dicarboxylic acids, aliphatic dicarboxylic acids, poly(alkylene ether) glycols, glycols, and components containing alkali metal or alkaline earth metal sulfo groups.

Description

technical field [0001] This invention relates to polyetherester films, coatings and laminates. More specifically, the present invention relates to sulfonated aliphatic-aromatic polyetheresters having superior thermal properties and being biodegradable. Background technique [0002] Inadequate treatment of municipal solid waste sent to landfills combined with the increasing addition of non-degradable materials, including plastics, to the municipal solid waste stream has resulted in a drastic reduction in the number of available landfills and the cost of municipal solid waste disposal increase. While recovery of reusable components of waste streams is desirable in many instances, recycling of these materials and the infrastructure required for recycling can sometimes be prohibitively expensive. Additionally, some products are not easily absorbed by the circular framework. Composting of non-recyclable solid waste is a recognized and growing method of reducing the volume of l...

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
Patent Type & Authority Patents(China)
IPC IPC(8): C08G63/688C08G63/672C08L67/02C08J5/18C09D167/02B32B27/06C08K3/00B32B27/36C08K3/34C08L3/02C08L67/04C08L69/00C08L77/12C08L101/16
CPCC08L3/02C08L69/00C08J2367/02C08L67/02C08L77/12C08K3/0033B32B27/06B32B27/36C08G63/6886C09D167/025C08G63/672C08K3/346C08L67/025C08L67/04C08J5/18C08K3/013C08L2666/02C08L2666/18B32B7/12B32B5/18B32B2553/00B32B27/10B32B27/20B32B27/08B32B2307/516B32B2307/518B32B2305/30B32B2317/12B32B2439/62B32B2439/60B32B2439/70
Inventor R·A·海斯L·J·皮克J·M·施奈德
Owner EI DU PONT DE NEMOURS & CO