Osterlene® LLB100 (-B, -SA, -SAM)
Osterman & Company - Linear Low Density Polyethylene Monday, May 27, 2024
General Information
Product Description
• LLB100 is a general-purpose film grade linear low density polyethylene. This resin exhibits excellent toughness and strength when drawn down to
thin gauges.
• Suggested applications for LLB100 include blending resin applications, industrial packaging, co-extrusion and industrial liners. Uses include bags,
liners and packaging.
General
Material Status • Commercial: Active
• Africa & Middle East • Europe
Availability
• Asia Pacific • Latin America
Additive • -B: Antiblock: No; Slip: No • -SA: High Antiblock; High Slip • -SAM: Medium Antiblock;
Medium Slip
• Butene Comonomer • High Strength
Features
• General Purpose • High Toughness
• Bags • Liners
Uses
• Blending • Packaging
Processing Method • Extrusion
ASTM & ISO Properties 1
Physical Nominal Value Unit Test Method
Density 0.919 g/cm³ ASTM D1505
Melt Mass-Flow Rate (MFR) (190°C/2.16 kg) 1.0 g/10 min ASTM D1238
Films Nominal Value Unit Test Method
Tensile Strength - MD (Break) 6200 psi ASTM D882
Tensile Strength - TD (Break) 4700 psi ASTM D882
Tensile Elongation - MD (Break) 540 % ASTM D882
Tensile Elongation - TD (Break) 800 % ASTM D882
Dart Drop Impact 75 g ASTM D1709
Elmendorf Tear Strength - MD 120 g ASTM D1922
Elmendorf Tear Strength - TD 350 g ASTM D1922
Optical Nominal Value Unit Test Method
Gloss (45°) 40 ASTM D2457
Haze 18.0 % ASTM D1003
Legal Statement
Contact your Osterman Customer Service Representative for potential food contact application compliance (e.g. FDA, EU, HPFB).
Notes
1
Typical properties: these are not to be construed as specifications.
LEGAL DISCLAIMER: Before using a product sold by Osterman, 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.
