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Comprehensive Rheological Characterization to Optimize Electrode Manufacturing

Summary Electrode manufacturing for lithium-ion batteries is a complex, multistep process that requires comprehensive material characterization to ensure quality and consistency in the final electrodes. Electrode processing involves combining active materials with binders and conductive additives to form a coating on the current collector, either as a slurry or dry coating. The mixing and coating…

Unlocking Data Accessibility with TRIOS JSON Export

Unlocking Data Accessibility with TRIOS JSON Export

Overview We’re excited to introduce a brand-new feature in TRIOS called TRIOS JSON (JavaScript Object Notation) Export. Whether you’re deep into data science, streamlining automation, or simply seeking better ways to archive your results, JSON Export will transform the way you use your TRIOS data. Download the TRIOS JSON Schema: https://software.tainstruments.com/schemas/TRIOSJSONExportSchema Check out our Python…

TRIOS EasyMass: Unlocking Efficient Experiment Preparation with Automatic Mass Data Transfer

TRIOS EasyMass: Unlocking Efficient Experiment Preparation with Automatic Mass Data Transfer

Overview Learn how to use the new TRIOS EasyMass feature for the TA Instruments Discovery DSC (Differential Scanning Calorimeter), which allows you to automatically send mass data from your balance directly to TRIOS. The balance is connected directly to a computer by a USB cable, and on-screen instructions guide users through the sample weighing process.…

Syringe and needle with glass medical ampoule vials for injection. Medicine is dry white drug penicillin powder or liquid with of aqueous solution in ampulla

Unlocking Stability: The Crucial Role of Thermal Analysis in Lyophilization Temperature Optimization

The method of drug delivery significantly influences the final stages of the manufacturing process. Currently, lyophilization—a widely adopted technique—enables drug developers to stabilize formulations and therapeutic molecules using a validated commercial approach. In this process, precise control of pressure and temperature within a lyophilizer facilitates the removal of liquids from formulations containing thermally sensitive or hydrolytically unstable active pharmaceutical ingredients or formulation components.