About |
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Versaflex™ CL E90 is an exceptional clarity, high performance and autoclavable solution ideal for healthcare and food packaging. Versaflex™ CL E90 is also formulated without the use of plasticizers. New Product. Commercial specifications have not been established. Flexible Formulated without Plasticizers High Clarity&& |
Product Description | |
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Supplier | Polyone |
Generic | TPE |
Material Status | Commercial: Active |
Features | Good Clarity,Good flexibility |
Availabilitys | Africa & Middle East ,North America,Latin America,Asia Pacific |
Process Methods | Extrusion |
Technical Data | |||
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MECHANICAL | Nominal value | Unit | Test method |
Shore hardness | |||
Shore A, 10 seconds | 90 | ASTM D2240 |
film | Nominal value | Unit | Test method |
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Oxygen permeability | ASTM D3985 | ||
21℃,120 µm | 280 | cm³·mm/m²/atm/24 hr | ASTM D3985 |
21℃,1800 µm | 260 | cm³·mm/m²/atm/24 hr | ASTM D3985 |
Oxygen transfer rate | ASTM D3985 | ||
21℃,120 µm | 2300 | cm³/m²/24 hr | ASTM D3985 |
21℃,1800 µm | 140 | cm³/m²/24 hr | ASTM D3985 |
elastic body | Nominal value | Unit | Test method |
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tensile strength | ASTM D412 | ||
Fracture, 23 ℃ | 12.6 | MPa | ASTM D412 |
100% strain, 23 ℃ | 6.89 | MPa | ASTM D412 |
300% Strain, 73°F | 8.51 | MPa | ASTM D412 |
Tensile strain | |||
Fracture, 23 ℃ | 570 | % | ASTM D412 |
Compression deformation | ASTM D395B | ||
22℃,22 hr | 27 | % | ASTM D395B |
70℃,22 hr | 67 | % | ASTM D395B |
100℃,22 hr | 73 | % | ASTM D395B |
PHYSICAL | Nominal value | Unit | Test method |
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Density | 0.898 | g/cm³ | ASTM D792 |
Apparent viscosity of melt | ASTM D3835 | ||
200℃,1340 sec^-1 | 162 | Pa·s | ASTM D3835 |
200℃,11200 sec^-1 | 34.0 | Pa·s | ASTM D3835 |
Process Conditions | |||
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Extrusion | Nominal value | Unit | Test method |
Melt temperature | 182 to 204 | °C | |
Nozzle temperature | 171 to 199 | °C |
Notes |
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1. Please contact GLS Thermoplastic Elastomers for a copy of the FDA compliance letter. |
2. Please contact PolyOne GLS Thermoplastic Elastomers for a complete copy of the GLS Healthcare Policy. 1. The Customer must notify GLS of any FDA Class I and/or European Union Class I medical devices for each specific product and application. 2. The Customer shall not knowingly manufacture, use, sell or otherwise supply, directly or indirectly products or compounds made from GLS products in any of the following without prior written approval by GLS for each specific product or application: a. Cosmetics b. Drugs and other Pharmaceuticals c. Temporary or permanent implantation in the human body, regardless of the intended duration of implantation d. Class II and Class III Medical Devices as defined in 21 CFR 860.3 (“Medical Devices”) e. Class IIa, IIb and III as defined in Directive 93/42/EEC |
3. Typical properties: these are not to be construed as specifications. |
4. Die C |
5. 2 hr |
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