Versaflex™ CL2250

About
Versaflex™ CL2250 is an easy processing compound designed for use in injection molding applications where FDA compliance, clarity and enhanced heat resistance are required. Excellent Clarity Overmold Adhesion to Polypropylene Superior Colorability Very Good Heat and Boil Resistance&&

Product Description
SupplierPolyone
GenericTPE
Material StatusCommercial: Active
FeaturesExcellent Processability,Good Clarity,Good coloring
AvailabilitysAfrica & Middle East ,North America,Latin America,Asia Pacific
Process MethodsInjection Molding

Technical Data
elastic bodyNominal valueUnitTest method
tensile strength ASTM D412
Fracture, 23 ℃5.70MPaASTM D412
100% strain, 23 ℃1.52MPaASTM D412
300% Strain, 73°F2.32MPaASTM D412
Tensile strain
Fracture, 23 ℃770%ASTM D412
tear strength24.5kN/mASTM D624
Compression deformation
23℃,22 hr20%ASTM D395B

MECHANICALNominal valueUnitTest method
Shore hardness
Shore A, 10 seconds50 ASTM D2240
Bending modulus13.9MPaASTM D790

PHYSICALNominal valueUnitTest method
Density0.888g/cm³ASTM D792
Melt Flow Rate
190℃,2.16kg13g/10minASTM D1238
Shrinkage rate
MD0.80 to 1.2%ASTM D955
Apparent viscosity of melt
200℃,11200 sec^-111.9Pa·sASTM D3835

Process Conditions
injectionNominal valueUnitTest method
Proposed maximum recycled material ratio20%
Barrel rear temperature171 to 188°C
Barrel middle temperature193 to 221°C
Barrel front temperature193 to 227°C
Nozzle temperature210 to 227°C
Processing (melt) temperature210 to 221°C
Mold temperature13 to 38°C
Back pressure0.00 to 0.552MPa
Screw speed25 to 75rpm

Notes
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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