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公开(公告)号:US10766832B1
公开(公告)日:2020-09-08
申请号:US16004098
申请日:2018-06-08
发明人: Jacob M Laktas , Ian D Stochl , Gregory J Place , Paul Jelliss , Stephen Chung , Steven W Buckner
摘要: The present invention generally concerns a nano-enhanced explosive that is integrated at many points across an explosive train. More specifically, a nano-enhanced explosive is formed when a nanocomposite we call nMx is combined with a secondary high explosive. nMx is made of Li3AlH6 nanoparticles, elemental Al nanoparticles, an amount of Ti metal, and a nanoscale organic layer having unique burning profiles that lend energy to the explosive process including increased shockwave propagation through a chemical explosive and increased temperatures and gaseous pressure build up and release in and about the same. Our nano-enhanced explosive can be integrated at various points across an explosive train, e.g. use within a detonation cord (fuse), or as a detonation charge (initiator), or as the main charge, where the use of the nano-enhanced explosive can be characterized by the energy lent to projectiles from munitions, bubbles formed by underwater explosive trains, or blast profiles.
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公开(公告)号:US11672875B2
公开(公告)日:2023-06-13
申请号:US17204524
申请日:2021-03-17
CPC分类号: A61K49/0404 , A61K49/0428 , A61K49/0002 , B82Y5/00 , C08L5/04
摘要: Disclosed are capped nanoparticles that are effectively trapped within an aqueous gelling solution to produce stable gels and function as a contrast agent for vascular imaging. The contrast agent has good radioopacity, is inexpensive to produce, and is safe to handle. This provides a new method to image the fine vasculature of biological systems.
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公开(公告)号:US20220296732A1
公开(公告)日:2022-09-22
申请号:US17204524
申请日:2021-03-17
IPC分类号: A61K49/04
摘要: Disclosed are capped nanoparticles that are effectively trapped within an aqueous gelling solution to produce stable gels and function as a contrast agent for vascular imaging. The contrast agent has good radioopacity, is inexpensive to produce, and is safe to handle. This provides a new method to image the fine vasculature of biological systems.
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