Hifax CA 212 A is a reactor TPO (thermoplastic polyolefin) manufactured using the LyondellBasell’ s proprietary Catalloy process technology.
It has been developed for industrial applications where a combination of good processability and excellent softness is required.
The grade is available in natural pellet form.
Hifax CA 212 A
Description
Availability
Asia-Pacific, Australia and New Zealand, Europe, North America, South & Central America
Legend
SDS - Safety Data Sheet
PSB - Product Stewardship Bulletin
Product Data and Technical Information
| Melt Flow Rate (230 °C/2.16 kg) | 8 g/10 min |
| Density (23 °C, Method A) | 0.88 g/cm³ |
| Flexural Modulus | 80 MPa |
| Tensile Stress at Break | 10 MPa |
| Tensile Stress at Yield | 6 MPa |
| Tensile Elongation at Break | >600 % |
| Tensile Strain at Yield | >40 % |
| Charpy Impact Strength - Notched (23 °C) | NB kJ/m² |
| Charpy Impact Strength - Notched (-20 °C) | 105 kJ/m² |
| Charpy Impact Strength - Notched (-40 °C) | 4 kJ/m² |
| Shore Hardness (Shore D) | 30 |
| Vicat Softening Temperature (A50) | 56 °C |
| Deflection Temperature Under Load (0.45 MPa, Unannealed) | 40 °C |
| Melting Temperature | 142 °C |
Technical Data Sheet
Technical Data SheetProcess
Calendaring, Compounding, Extrusion Coating, Injection Molding, Sheet
Resin
Catalloy
Applications
Automotive Flooring, Polymer Modifier, Single Ply Roofing, TPO Foils and Skins
Prohibited Applications of Compounded Polyolefins:
The following applications and/or end uses are prohibited by LyondellBasell. LyondellBasell will not solicit the sale of, or knowingly supply, product for use in the following applications:
FDA Class III medical devices, European Class III medical devices, Health Canada Class IV Medical Devices, applications involving permanent implantation into the body & life-sustaining medical applications