Modified heterophasic polyolefin composition

Active Publication Date: 2016-01-28
MILLIKEN & CO
View PDF6 Cites 5 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0005]The invention generally provides heterophasic polymer compositions comprising a propylene polymer phase and an ethylene polymer phase. A compatibilizing agent is also added to the compositions. The addition of the compatibilizing agent to the compositions has been observed to preserve, or even improve, the impact resistance of the polymer composition when the melt flow rate of the polymer composition is increased by the use of a free radical generator.

Problems solved by technology

Increasing the melt flow rate by decreasing the molecular weight of the polyolefin polymer, however, has been found in many cases to have a detrimental effect on the strength of the modified polymer.
For example, decreasing the molecular weight of the polymer can significantly lower the impact resistance of the polymer.
And this lowered impact resistance can make the polymer unsuitable for use in certain applications or end uses.
Accordingly, when extant technologies are utilized, one must strike a compromise between increasing the melt flow rate and undesirably decreasing the impact resistance of the polymer.
This compromise often means that the melt flow rate is not increased to the desired level, which requires higher processing temperatures and/or results in lower throughputs.

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
  • Modified heterophasic polyolefin composition
  • Modified heterophasic polyolefin composition
  • Modified heterophasic polyolefin composition

Examples

Experimental program
Comparison scheme
Effect test

Example

Example 1

[0077]The following example demonstrates the modification of a heterophasic polyolefin composition and performance enhancements achieved, according to the method of the present invention.

[0078]Four heterophasic polymer compositions were produced. Comparative Sample 1A (C.S. 1A) was an unmodified polypropylene copolymer. Comparative Sample 1B (C.S. 1B) was made with the same polypropylene copolymer vis-broken using a peroxide. Samples 1A and 1B were made with the same vis-broken polypropylene copolymer compounded with 2-(furan-2-ylmethylene)malononitrile (Compound ID 1 from Table 7 below) as a compatibilizing agent. The general formulation for these samples is set forth in Table 1.

TABLE 1Heterophasic polypropylene copolymer formulationsComponentLoadingPolypropylene copolymerBalance(LyondellBasell Pro-Fax SD375S withapproximately 19% xylene solubles)Primary antioxidant (Irganox ® 1010)500 ppmSecondary antioxidant (Irgafos ® 168)1000 ppm Acid scavenger (calcium stearate)800 ppmPe

Example

Example 2

[0081]The following example investigates the effects of using a compatibilizing agent in a non-heterophasic polyolefin composition.

[0082]Four non-heterophasic polymer compositions were produced. Comparative Sample 2A (C.S. 2A) was an unmodified polypropylene polymer. Comparative Sample 2B (C.S. 2B) was made with the same polypropylene polymer vis-broken using a peroxide. Comparative Samples 2C and 2D were made with the same vis-broken polypropylene polymer compounded with 2-(furan-2-ylmethylene)malononitrile as a compatibilizing agent. The general formulation for these samples is set forth in Table 3.

TABLE 3Non-heterophasic polypropylene homopolymer formulationsComponentLoadingPolypropylene HomopolymerBalance(Total Petrochemicals 3276)Primary antioxidant (Irganox ® 1010)500 ppmSecondary antioxidant (Irgafos ® 168)1000 ppm Acid scavenger (calcium stearate)800 ppmPeroxide (Varox DBPH)See Table 4Additive (Compatibilizing Agent)See Table 42-(furan-2-ylmethylene)malononitrileIrgano

Example

Example 3

[0085]The following example demonstrates the production of several heterophasic polyolefin compositions as described above and investigates the performance enhancements achieved through the incorporation of the compatibilizing agents as described above.

[0086]In order to permit a comparison of the various compatibilizing agents and their effects on the physical properties of a heterophasic polymer composition, the relationship between melt flow rate and Izod impact of a commercially-available polypropylene copolymer (LyondellBasell Pro-Fax SD375S) was investigated by vis-breaking the polymer using several different loadings of a commercially-available peroxide (Varox BDPH). A compatibilizing agent according to the invention was not used in these compositions. The raw MFR and Izod impact values obtained from these measurements were then indexed to the MFR and Izod impact values of the virgin, unmodified polymer (not vis-broken) to provide relative values. The relative MFR and Iz

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
Temperatureaaaaaaaaaa
Fractionaaaaaaaaaa
Weightaaaaaaaaaa
Login to view more

Abstract

A heterophasic polymer composition comprises a propylene polymer phase, an ethylene polymer phase, and a compatibilizing agent. The compatibilizing agent comprises (i) an acyclic carbon-carbon double bond having a first carbon atom and a second carbon atom, (ii) an electron withdrawing group directly bonded to the first carbon atom in the acyclic carbon-carbon double bond, and (iii) a second carbon-carbon multiple bond in conjugation with the acyclic carbon-carbon double bond, wherein the second carbon-carbon multiple bond is linked to the acyclic carbon-carbon double bond through the second carbon atom.

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 MILLIKEN & 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