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T.O.M. Microfilm Reel 219

(Original designation Navy 5939-10)

Table of Contents

Note from the editors – only selected documents from this microfilm reel have been completely processed and presented below in cleaned and grouped format (Items 9 and 10, identified by HTML link below).  The remainder of the reel is not related to the Fischer-Tropsch process, and therefore complete processing cannot be justified at this time.

We are, however, making the entire reel contents available in raw image format, although in a small number of relatively large files (rather than a very large number of small individual images).  Anyone interested in pursuing the non-FT related material on this reel may find the document in these much larger raw files.

Images 0001-0109                 File size ca.  89 Mb

Images 0189-0250                 File size ca.  71 Mb

Images 0251-0306                 File size ca.  41 Mb

1.             Peroptan, a synthetic gasoline for aviation fuel, is the condensation product of npropyl chloride with isobutane.  The condensation is made in the presence of aluminum chloride and gives a branched, 7-carbon atom hydrocarbon for fuel purposes for air craft engines.

Peroptan is claimed to be made in 90 percent theoretical yield and to have an octane number of at least 98.  The propyl chloride used in the synthesis of peroptan is made from liquid chlorine and liquid propane in the presence of light.  Peroptan has a boiling range of 80 to 180° Centigrade.  Peroptan is said to be equal in octane reading to the gasoline produced by the alkylation process as practiced in Germany.

2.              Preparation of di-n-ketone peroxide.

3.             Graphite peroxide (C2O).

4.              Conference on gas manufacturing in Ludwigshafen:

Dehydrogenation of n-butane.

Dehydrogenation of isobutane.

Catalyst preparation.

Butylene concentration.

Isomerization of n-butane.

Alkylation of isobutane with various olefins.

BF3 and HF catalysts.

Alkylation of benzene.

Polymer gasolines.

5.             Recovery of propylene by catalytic stepwise dehydrogenation of butane-propane mixtures.

6.             Summary of a conference on gas manufacture at Leuna covering same topics as No. 4 above.

7.             Isomerization of n-butane of alumina chloride.

8.             Series of papers on carbon monoxide hydrogen reaction to alcohols and carbons.

9.             Experiments with iron catalysts for the Fischer-Tropsch reaction.

A.      Correspondence, short reports, and design economics relating to the (Duftschmid) oil-recycle process.  1940-1944.  19 pages.

B.       German patent application – unnumbered.  Process for the conversion of carbon monoxide with hydrogen (iron catalyzed Fischer-Tropsch process).  Ammoniaklaboratorium, Oppau.  March 23, 1944.  7 pages.

C.       German patent application – unnumbered.  Process for the production of carbon monoxide and hydrogen from hydrocarbons.  Ammoniaklaboratorium, Oppau.  June 13, 1940.  5 pages.

D.      Report on group leader conference of paraffin (iron catalyzed Ficher-Tropsch) synthesis.  Ludwigshafen am Rhein.  March 31, 1943.  6 pages – appears to be incomplete.

E.       Detailed data sheets from the Reichsamtversuche tests.  Braunkohle-Benzin, Schwarzheide.  1943.  6 pages.

F.       Correspondence, memos, run sheets/data, and flow/equipment sketches from the Reichsamtversuche.  1943.  16 pages.

G.       Memos and correspondence on the cobalt supply situation with regard to Fischer-Tropsch synthesis catalysts.  May, 1943.  12 pages.

10.           German patent application draft – unnumbered.  Method for the removal of fog, soot, and dust from gases.  January 13, 1942.  6 pages.

11.           Research on GM and combustible insulating materials and explosiveness of GM with Iporka, Desmosit and T. Kohle.

12.           An extensive survey of syntheses using acetylene as starting material.

13.            Preparation of high anti-knock gasoline by the alkylation of isobutane with butene-1, pilot-scale plant.

14.           Synthesis of fatty acid esters and fatty acids by the action of carbon monoxide with olefins and alcohols, and olefins and water.