Abstract: The processes and products described herein optimize transformation of BNNT as-synthesized material into BNNT intermediary materials. Process steps include refining to remove boron particulates, high temperature refining to break bonds between BNNT, h-BN nanocages, h-BN nanosheets and amorphous BN particles, centrifuging and microfluidic separation, and electrophoresis. Resultant BNNT intermediary materials include purified BNNT in solution, BNNT gels, h-BN nanocages, and h-BN nanosheets, gel spun BNNT fibers, hydrophilic defect enhanced BNNT materials, BNNT patterned sheets, and BNNT strands. Applications that will utilize these BNNT precursor feedstock materials include making BNNT based aligned components, thin films, aerogels, thermal conductivity enhancements, structural materials, ceramic, metal, and polymer composites, and removal of PFAS pollutants from water.

Abstract: The structural integrity and viscoelastic performance of boron nitride nanotube (BNNT) materials may be improved through forming a compressed BNNT buckyweave. The BNNT buckyweave may be formed from a BNNT buckypaper having a bulk nanotube alignment (partial alignment) that may be maintained when forming the BNNT buckyweave, and compression may be parallel to and/or perpendicular to the partial alignment. The BNNT material may be viscoelastically-enhanced through, e.g., selection of synthesized BNNT material, impurity removal/reduction, BNNT alignment, isotopically enhancement, and compression relative to alignment. BNNT buckyweave s are introduced. The present approach provides viscoelastic behavior over temperatures from near absolute zero to near 1900 K. The transport of phonons along the BNNT molecules may be enhanced by utilizing isotopically enhanced BNNTs.

Abstract: This disclosure relates to the use of hydrogen storage compounds in boron nitride nanotube (BNNT) fusion targets. Such targets may be used with high power pulsed laser beams to produce proton nB fusion reactions. BNNT fusion targets having a hydrogen storage compound (such as ammonia borane) coating, and methods for making the same, are disclosed.

Abstract: This disclosure relates to the use of hydrogen storage compounds and high atomic weight elements in boron nitride nano tube (BNNT) fusion targets. Such targets may be used as targets for high power pulsed laser beams to produce proton 11B fusion reactions. BNNT fusion targets having as additives a hydrogen storage compound (such as ammonia borane) and a high atomic weight element (such as xenon), and methods for making the same, are disclosed.

Abstract: Boron nitride nanotubes (BNNTs) having a second scintillating material, and in some embodiments an enhanced 10B content, may be used for efficient thermal neutron detection. The second scintillating material may be a crystal coating on the nanotubes, and/or crystal dispersed within the BNNT material. Crystal-coated BNNT materials enable detecting thermal neutrons by detecting light from the decay products of the thermal neutron’s absorption on the 10B atoms in the BNNT material, as the resultant decay products pass through the crystal-coating. Embodiments of thermal neutron detectors are described. Methods for preparing BNNTs with a second scintillating material are also described.

Abstract: Thermal interface materials may be enhanced through the dispersion of refined boron nitride nanotubes (BNNTs) into a polymer matrix material and one or more microfillers. A refined BNNT material may be formed by reducing free boron particle content from an as-synthesized BNNT material, and in some embodiments reducing h-BN content. Reducing these species improves the thermal conductivity of the BNNTs. Refined BNNTs may be deagglomerated to reduce the size and mass of BNNTs in agglomerations when the deagglomerated BNNT material is dispersed into a target polymer matrix material. The deagglomerated BNNT material may be lyophilized prior to dispersion in the matrix material, to retain the deagglomeration benefit following return to solid state. The surface of the deagglomerated BNNT material may be modified, with one or more functional groups that improve dispersibility and heat transfer in the target polymer matrix material.

Abstract: Thermal interface materials may be enhanced through the dispersion of refined boron nitride nanotubes (BNNTs) into a polymer matrix material and one or more microfillers. A refined BNNT material may be formed by reducing free boron particle content from an as-synthesized BNNT material, and in some embodiments reducing h-BN content. Reducing these species improves the thermal conductivity of the BNNTs. Refined BNNTs may be deagglomerated to reduce the size and mass of BNNTs in agglomerations when the deagglomerated BNNT material is dispersed into a target polymer matrix material. The deagglomerated BNNT material may be lyophilized prior to dispersion in the matrix material, to retain the deagglomeration benefit following return to solid state. The surface of the deagglomerated BNNT material may be modified, with one or more functional groups that improve dispersibility and heat transfer in the target polymer matrix material.

Abstract: The structural integrity and viscoelastic performance of boron nitride nanotube (BNNT) materials may be improved through forming a compressed BNNT buckyweave. The BNNT buckyweave may be formed from a BNNT buckypaper having a bulk nanotube alignment (partial alignment) that may be maintained when forming the BNNT buckyweave, and compression may be parallel to and/or perpendicular to the partial alignment. The BNNT material may be viscoelastically-enhanced through, e.g., selection of synthesized BNNT material, impurity removal/reduction, BNNT alignment, isotopically enhancement, and compression relative to alignment. BNNT buckyweave s are introduced. The present approach provides viscoelastic behavior over temperatures from near absolute zero to near 1900 K. The transport of phonons along the BNNT molecules may be enhanced by utilizing isotopically enhanced BNNTs.

Abstract: Thermal interface materials may be enhanced through the dispersion of refined boron nitride nanotubes (BNNTs) into a polymer matrix material and one or more microfillers. A refined BNNT material may be formed by reducing free boron particle content from an as-synthesized BNNT material, and in some embodiments reducing h-BN content. Reducing these species improves the thermal conductivity of the BNNTs. Refined BNNTs may be deagglomerated to reduce the size and mass of BNNTs in agglomerations when the deagglomerated BNNT material is dispersed into a target polymer matrix material. The deagglomerated BNNT material may be lyophilized prior to dispersion in the matrix material, to retain the deagglomeration benefit following return to solid state. The surface of the deagglomerated BNNT material may be modified, with one or more functional groups that improve dispersibility and heat transfer in the target polymer matrix material.

Abstract: Thermal interface materials may be enhanced through the dispersion of refined boron nitride nanotubes (BNNTs) into a polymer matrix material and one or more microfillers. A refined BNNT material may be formed by reducing free boron particle content from an as-synthesized BNNT material, and in some embodiments reducing h-BN content. Reducing these species improves the thermal conductivity of the BNNTs. Refined BNNTs may be deagglomerated to reduce the size and mass of BNNTs in agglomerations when the deagglomerated BNNT material is dispersed into a target polymer matrix material. The deagglomerated BNNT material may be lyophilized prior to dispersion in the matrix material, to retain the deagglomeration benefit following return to solid state. The surface of the deagglomerated BNNT material may be modified, with one or more functional groups that improve dispersibility and heat transfer in the target polymer matrix material.

Abstract: Thermal interface materials may be enhanced through the dispersion of refined boron nitride nanotubes (BNNTs) into a polymer matrix material and one or more microfillers. A refined BNNT material may be formed by reducing free boron particle content from an as-synthesized BNNT material, and in some embodiments reducing h-BN content. Reducing these species improves the thermal conductivity of the BNNTs. Refined BNNTs may be deagglomerated to reduce the size and mass of BNNTs in agglomerations when the deagglomerated BNNT material is dispersed into a target polymer matrix material. The deagglomerated BNNT material may be lyophilized prior to dispersion in the matrix material, to retain the deagglomeration benefit following return to solid state. The surface of the deagglomerated BNNT material may be modified, with one or more functional groups that improve dispersibility and heat transfer in the target polymer matrix material.