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Lagow, Richard J.

Publications and source records attributed to Lagow, Richard J..

Spherical Perfluoropolyethers

Four fluorocarbon compounds of generic class C(CF2OR)4 {where R = CF3, C(CF3)3, CF2CF3, or CF2CF2CF3} synthesized by direct fluorination of corresponding hydrocarbons. Molecules of these compounds approximately spherical and act as "molecular ball bearings." In addition to potential utility as lubricants, compounds expected thermally stable and useful as heat-transfer fluids or even vapor-phase-soldering fluids.

Lagow, Richard J.

Synthesis Of Perfluoro Orthocarbonates

Perfluoro tetraalkyl orthocarbonates and perfluoro dialkyl acetals synthesized by direct fluorination of orthocarbonates and polyalkoxy propanes. Perfluoro compounds more volatile than perfluoropolyethers having same molecular weights and stable at temperatures up to at least 150 degrees C. Useful as heat-exchange fluids, lubricants, and/or vapor-phase soldering fluids.

Lagow, Richard J.

The development of new, low-cost perfluoroalkylether fluids with excellent low and high-temperature properties

A series of perfluoroalkylether (PFAE) fluids were synthesized by direct fluorination. Viscosity-temperature properties, oxidation stabilities, oxidation-corrosion properties, and lubricity were determined. The fluids were tested in the presence of common elastomers to check for compatibility. The bulk modulus of each was measured to determine if any could be used as nonflammable aircraft hydraulic fluid. It was determined that as the carbon to oxygen ratio decreases, the viscometric properties improve, the fluids may become poor lubricants, the bulk modulus increases, the surface tension increases, and the fluid density increases. The presence of difluoromethylene oxide units in the polymer does not seriously lower the oxidation and oxidation-corrosion stabilities as long as the difluoromethylene oxide units are separated by other units.

Bierschenk, Thomas R.

The preparation of new perfluoro ether fluids exhibiting excellent thermal-oxidative stabilities

A series of low molecular weight perfluoroalkyl ethers (PFAEs) were synthesized by direct fluorination. Viscosity-temperature properties and oxidation stabilities were determined. Viscosity-temperature correlations indicated that increases in branching and increases in the size of the branching substituent caused a deterioration in viscometric properties (i.e., an increase in ASTM slope). In addition, increasing the ratio of carbon to oxygen in these compounds also increased the ASTM slope. Preliminary oxidation stability measurements indicated that highly branched PFAE fluids (i.e., those containing quaternary carbons) may be less stable than either those containing a single trifluoromethyl pendant group or those containing no branching at all.

Jones, William R., Jr.