B01J41/00

METHOD FOR THERMAL PRECONDITIONING OF NATURAL GRAPHITE FLAKES USING ELECTROMAGNETIC WAVES

An apparatus for processing graphite particles is disclosed. The apparatus may comprise an electromagnetic radiation emitting device including a microwave device coupled to the reaction chamber for the creation of electromagnetic waves, the electromagnetic waves comprising microwaves. The apparatus may also comprise an inlet attached to the reaction chamber for introducing graphite particles, and an outlet attached to the reaction chamber for allowing processed graphite particles to exit the reaction chamber. The graphite particles in the reaction chamber thermally altered by exposure to the electromagnetic radiation such that the graphite particles are heated

Polymerized ionic liquid block copolymers as battery membranes

The present invention is directed to compositions useful for use in separators for use in lithium ion batteries, and membranes, separators, and devices derived therefrom.

Polymerized ionic liquid block copolymers as battery membranes

The present invention is directed to compositions useful for use in separators for use in lithium ion batteries, and membranes, separators, and devices derived therefrom.

Ion exchange membrane filling composition, method of preparing ion exchange membrane, ion exchange membrane, and redox flow battery

A composition for filling an ion exchange membrane, a method of preparing the ion exchange membrane, the filled ion exchange membrane, and a redox flow battery using the filled ion exchange membrane. The composition includes an ion conductive material and a water soluble support.

Ion exchange membrane filling composition, method of preparing ion exchange membrane, ion exchange membrane, and redox flow battery

A composition for filling an ion exchange membrane, a method of preparing the ion exchange membrane, the filled ion exchange membrane, and a redox flow battery using the filled ion exchange membrane. The composition includes an ion conductive material and a water soluble support.

End-to-End Continuous Purification System
20220168668 · 2022-06-02 ·

An automated end-to-end continuous purification system for the manufacture of therapeutic proteins to reduce complexity of manual process operations and minimize physical space requirements.

Liquid absorber, liquid absorbing unit, and liquid ejection apparatus
11167554 · 2021-11-09 · ·

A liquid absorber includes a plurality of small chips. Individual ones of the small chips include a first substrate containing fibers, a second substrate containing fibers, and an absorbent resin supported between the first substrate and the second substrate. The first substrate contains an ion scavenger.

Device and cassette for performing a plurality of synthesis processes of preparing a radiopharmaceutical in series

A cassette for performing a plurality of synthesis processes of preparing a radiopharmaceutical in series in a synthesizer, includes: at least one manifold provided with a plurality of valves connectable to and operable by the synthesizer; an anion-exchanger comprising an anionic exchange material; an eluent container comprising an eluent; and a recondition container comprising a reconditioning agent.

Device and cassette for performing a plurality of synthesis processes of preparing a radiopharmaceutical in series

A cassette for performing a plurality of synthesis processes of preparing a radiopharmaceutical in series in a synthesizer, includes: at least one manifold provided with a plurality of valves connectable to and operable by the synthesizer; an anion-exchanger comprising an anionic exchange material; an eluent container comprising an eluent; and a recondition container comprising a reconditioning agent.

Generation of data for use with antimicrobials
11154853 · 2021-10-26 · ·

An assay is performed so as to identify a pathogen in a sample taken from a patient. The identity of the pathogen in the patient sample is used to select an antimicrobial for treatment of the patient. The antimicrobial can be selected in less than 7 hours after the patient sample is taken from the patient. For instance, when the sample is blood, the antimicrobial can be selected in less than 7 hours after the patient sample is taken from the patient. When the sample is urine, the antimicrobial can be selected in less than 4 hours after the patient sample is taken from the patient.