Test Method used
|Blown Film, Extrusion Blow Molding, Tapes & Raffia|
|Good Heat Aging Resistance , Good Impact Resistance , Low Temperature Impact Resistance, Good Melt Strength , Good Stiffness|
Typical Customer Applications
|Film Wrap, Food Packaging Film, Raffia/Tapes/Strapping, Under-the-Hood & Structural Applications|
|Melt Flow Rate (230°C/2.16kg)||ASTM D 1238||0.45||g/10 min|
|Density (23°C)||ISO 1183||0.90||g/cm³|
|Note: Method A|
|Tensile Stress at Yield (23 °C)||ISO 527-1, -2||26||MPa|
|Tensile Strain at Yield (23 °C)||ISO 527-1, -2||11||%|
|Flexural modulus (23 °C)||ISO 178||1180||MPa|
|Charpy notched impact strength||ISO 179|
|Notched izod impact strength||ISO 180|
|Heat deflection temperature B (0.45 MPa) Unannealed||ISO 75B-1, -2||78||°C|
|Heat deflection temperature A (1.80 MPa) Unannealed||ISO 75A-1, -2||49||°C|
|Typical properties; not to be construed as specifications.|
|© LyondellBasell Industries Holdings, B.V. 2014|
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Before using a product sold by a company of the LyondellBasell family of companies, users should make their own independent determination that the product is suitable for the intended use and can be used safely and legally. SELLER MAKES NO WARRANTY; EXPRESS OR IMPLIED (INCLUDING ANY WARRANTY OF MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE OR ANY WARRANTY) OTHER THAN AS SEPARATELY AGREED TO BY THE PARTIES IN A CONTRACT.
This product(s) may not be used in: (i) any U.S. FDA Class I, Health Canada Class I, and/or European Union Class I medical devices, without prior notification to Seller for each specific product and application; or (ii) the manufacture of any of the following, without prior written approval by Seller for each specific product and application: U.S. FDA Class II Medical Devices; Health Canada Class II or Class III Medical Devices; European Union Class II Medical Devices; film, overwrap and/or product packaging that is considered a part or component of one of the aforementioned medical devices; packaging in direct contact with a pharmaceutical active ingredient and/or dosage form that is intended for inhalation, injection, intravenous, nasal, ophthalmic (eye), digestive, or topical (skin) administration; and tobacco related products and applications. Additionally, the product(s) may not be used in: (i) U.S. FDA Class III Medical Devices; Health Canada Class IV Medical Devices; European Class III Medical Devices; (ii) applications involving permanent implantation into the body; (iii) life-sustaining medical applications; and (iv) lead, asbestos or MTBE related applications. All references to U.S. FDA, Health Canada, and European Union regulations include another country’s equivalent regulatory classification.
Users should review the applicable Material Safety Data Sheet before handling the product.
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Release Date: 30 Jan 2014