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ÊÇ·ñ½ø¿Ú£º·ñ | ³§¼Ò(²úµØ)£ºZG | ÅÆºÅ£º 2406MT GF20 |
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CELANEX 2406MT GF20 CFR 21 (177.1660) of the Food and Drug Administration (FDA) and is listed in the Drug Master File (DMF 10047 (US) / 10033 (EU)) and the Device Master File (MAF 443 (US) / 1078 (EU)) the corresponding EU and national registry regulatory requirements biocompatibility in tests corresponding to USP 23 Class VI/*** 10993 low residual monomers no animal products Product information Rheological properties Mechanical properties Thermal properties Flammability Physical/Other properties Injection To minimize the volatile content in the final product, dry the resin to ≤0.01% water content. In injection molding, use the lowest possible melt temperature (recommended 240 °C) and shortest feasible residence time (recommended 2-3 minutes). Store the parts in a ventilated, clean area before use. If assistance is needed please contact your Celanese account representative. Pre-Drying Diagrams
Celanex 2406MT GF20 is a special grade developed for medical industry applications and complies with:
These recommendations are based on internal Celanese testing. For drying and injection molding conditions outside the above parameters, customer must test for and verify suitably low volatiles emissions on molded articles to confirm the final product is suitably pure for its intended use.
To avoid hydrolytic degradation during processing, CELANEX resins have to be dried to a moisture level equal to or less than 0.01%. Drying should be done in a dehumidifying hopper dryer capable of dewpoints <-40°C (-40°F) at 140°C (284°F) for 4-6 hours.
Storage
For subsequent storage of the material in the dryer until processed (<= 60 h) it is necessary to lower the temperature to 100° C.
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