Development of battery separator material process Mid-program report
Heat sterilizable battery separator material prepared from low-density polyethylene film
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Heat sterilizable battery separator material prepared from low-density polyethylene film
Polymer separator materials for heat sterilizable battery
Fabrication and testing of battery separator material of modified polyethylene film
Inorganic separator for high temperature silver-zinc battery
Filler and matrix composite materials for use in silver-zinc battery separators
Fabrication and test of polyethylene base material for heat sterilization resistance and for battery separators in silver-zinc alkaline cell
Polyphenylene oxide case and cover mechanical properties determination, and component reliability tests for silver-zinc battery with inorganic separators
Coating procedure for tape separator of heat sterilizable battery
Performance testing of alkaline battery separator films
Silver zinc battery separator material development and production
Ethylene/acrylic acid separators for silver zinc battery applications
Cycling tests of alkaline battery separator membranes
Membrane and absorber screening tests for alkaline battery separators
Ethylene/methyl acrylate copolymer synthesis for silver-zinc battery separators
Ionic transport characteristics of ionenes, insoluble membranes from soluble polyelectrolyte compositions, are studied for possible application in a battery separator. Effectiveness of the thin film of separator membrane essentially determines battery lifetime.
Absorber evaluation of alkaline battery separator systems with electrolyte wetting and wicking measurement
Abstract Lanthanide‐binding tag (LBT) peptides selectively complex lanthanide cations (Ln 3+ ) in their binding pockets and are promising for lanthanide separation. However, designing LBTs that selectively target specific Ln 3+ cations remains a challenge due to limited molecular‐level understanding and control of interactions within the lanthanide‐binding pocket. In this study, we reveal that the N5 asparagine residue acts as a gatekeeper in the binding pocket, resulting in a 100‐fold selectivity for smaller Lu 3+ over larger La 3+ cations. Nuclear magnetic resonance spectroscopy and molecular dynamics simulations show that the N5 residue weakly binds to the larger La 3+ cation, permitting H 2 O molecules inside the pocket. For the smaller Lu 3+ cations, the N5 residue forms an inter‐arm hydrogen bond with the E14 glutamic acid residue, locking the Lu 3+ cation in the pocket and preventing H 2 O infiltration. Mutating the N5 asparagine to a D5 aspartic acid prevents such a hydrogen bond, eliminating the gatekeeping mechanism and precipitously reducing selectivity. The resulting binding affinity to Ln 3+ cations is non‐monotonic but generally increases with cation size. These results suggest a molecular design paradigm: the reduced affinity for larger lanthanides is due to open pocket conformations, while the selectivity of smaller Ln 3+ cations over larger ones is due to the gatekeeping hydrogen bond.
Physical and chemical stability, transport properties, and battery performance in simplified cell design for alkaline silver battery separator materials