RESEARCH ON LOW TEMPERATURE FUEL CELL SYSTEMS

Abstract

Comparative reactivities of a group of saturated hydrocarbons were determined in Pt anode fuel cells containing both strongly acidic and strongly basic electrolytes at 25 to 65 C. Rough values of activation energy for the over-ALL OXIDAION PROCESSES WERE CALCULATED FOR HIGH REACTIVITIES. Measurements with the series CH4, C2H6, C3H8, isobutane, neopentane show that the tertiary H in iobutane does not produce any noticeable enhancement in the anodic reactivity of this molecule. Gavanostatic studies of CH4, C2H6, C3H8, isobutane, ethylene and cyclopropane indicate that the rate of adsorption of saturated hydrocarbons on Pt black electrodes is markedly dependent upon the electrolyte. Slow adsorption occurs in the presence of bicarbonate and caustic. Ethylene and cyclopropane are more readily adsorbed than the saturated hydrocarbons, and both gases adsorb readily in the presence of acidic caustc and bicarbonate electrolytes. Steps attributale to adsorbed H appear on the saturated hydrocarbon galvanostatic oxidation curves. The adsorbed carbonaceous species from the hydocarbons require high overvoltages for their oxidation.

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Document Details

Document Type
Technical Report
Publication Date
Sep 30, 1961
Accession Number
AD0268235

Entities

Organizations

  • General Electric

Tags

Communities of Interest

  • Air Platforms
  • Human Systems

DTIC Thesaurus Topics

  • Alkanes
  • Alkenes
  • Army
  • Chemical Reactions
  • Chemical Synthesis
  • Chemistry
  • Current Density
  • Fuel Cells
  • Gaseous Fuels
  • Hydrocarbon Fuels
  • Hydrocarbons
  • Hydrogen Bonds
  • Materials
  • Materials Processing
  • Materials Science
  • Measurement
  • Organic Chemistry

Fields of Study

  • Chemistry

Readers

  • Electrochemical Engineering/ Fuel Cell Technologies
  • Organic Chemistry

Technology Areas

  • Biotechnology