Energy recuperation: Difference between revisions

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'''Energy recuperation on the single bond level:'''
== Energy recuperation on the single bond level ==
 
* energy recuperation in [[piezochemical mechanosynthesis]]  
* energy recuperation in [[piezochemical mechanosynthesis]]  
* energy recuperation in the [[drive subsystem of a gem-gum factory]] – e.g. in [[chemomechanical conversion]]
* energy recuperation in the [[drive subsystem of a gem-gum factory]] – e.g. in [[chemomechanical conversion]]
See: [[Dissipation sharing]] – (Related: [[Exothermy offloading]])
See: [[Dissipation sharing]] – (Related: [[Exothermy offloading]])


'''Energy recuperation on small scales:'''
'''Potential waste heat increasing factors:'''
* Higher energy turnover due to more surface area broken open and reformed again
* Higher energy turnover due to [[covalent bonds]] being significantly stronger than [[Van der Waals bonds]]
* Possibly less highly optimizable for efficiency due to localized high strains being unavoidable – (related: [[back driving]] a gear-train)
 
== Energy recuperation on small scales ==
 
* energy recuperation from [[Van der Waals bonds]]
* energy recuperation from [[Van der Waals bonds]]
* energy recuperation from [[superelastic]] clips, avoiding larger scale [[snapback]]
* energy recuperation from [[superelastic]] clips, avoiding larger scale [[snapback]]

Revision as of 15:53, 13 June 2021

This article is a stub. It needs to be expanded.

Energy recuperation on the single bond level

See: Dissipation sharing – (Related: Exothermy offloading)

Potential waste heat increasing factors:

  • Higher energy turnover due to more surface area broken open and reformed again
  • Higher energy turnover due to covalent bonds being significantly stronger than Van der Waals bonds
  • Possibly less highly optimizable for efficiency due to localized high strains being unavoidable – (related: back driving a gear-train)

Energy recuperation on small scales

Related