T.O.M. Microfilm Reel 285
(Original Designation FIAT Reel J-281)
Table of Contents
Continued from TOM reel 284
Documents taken from Henkel & Cie, Düsseldorf
Item
A. Work Carried out:
1. Preparation of iso-butylphenol. Page2.
2. Preparation of iso-dodecyl-p-phenol chloride. Page.
3. Preparation of di-isobutyl-o-cresol. Page 5.
4. Preparation of di-isobutyl-p-phenol chloride. Page 7.
5. Investigation of the reaction of 1, 10 decanediol with p-phenol chloride. Page 9.
6. Experiments on the preparation of cyclohexyl phenylpropylacohol. (Patent example.) Page 10
7. Preparation of dodecene. Page 13.
8. Sulfonation of dodecyl-o-cresol and octyl-o-cresol. Page 13.
9. Investigation of gasoline, condensation to "Saptenols" (using cresol and perchloric acid) and hydrogenation of "Saptenols" to "Saptols." Page 14.
a. Crack gasoline A, Holland.
b. Crack gasoline B, Holland
c. Crack gasoline, Deurag.
d. Crack gasoil, Deurag, June 1, 1935.
e. Crack gasoil, Deurag, June 27, 1935.
B. Current work:
1. Hydrogenation of "Saptenols" and sulfonation of "Saptols." Page 40a.
2. Condensation of crack gasoil, with cresol. Page 44.
(Graphs and tables included in report.)
A. Work carried out:
1. Preparation and yield of "Saptenol" 531. (See Zwischenbericht of Sept. 14 and Sept. 27, 1935).
2. Soapstock-whale oil fatty acid distillation. (See Zwischenbericht of Sept. 20, 1935.)
3. Determination of the corrosion resistance of copper in the preparation of "Saptenol." Page 2.
4. Treatment of crack gasoil, distillation condensation. Page 5.
5. Treatment of crack gasoil with perchloric acid. Page 7.
6. Treatment of Deurag crack gasoline with perchloric acid. Page 8.
7. Treatment of Deurag crack gasoline with perchloric acid and xylol. Page 8
(Items 1 and 2 in Group A are not included in report.)
B. Current work:
1. Preparation of perhydro-dicresylmethane-boric acid ester.
2. Investigation of the unsulfonated part of "Saptol", preparation of "Saptol" esters, adhesive substances and lubricant-like products. Page 12.
3. Preparation of "Saptenol" and "Saptol" from Ersag crack gasoline
(Items 1 and 3 in Group B are not included in report, but a section on the sulfur content and de-sulfurization of "Saptenols" appears, beginning on page 10.)
A. Work carried out:
1. Paraffin oxidation. (See Zwischenbericht of Feb. 21, 1936.)
2. Paraffin oxidation. Experiments on the control of results obtained in Item 1. Page 2.
3. Oxidation of hard paraffin. Page 11.
4. Treatment of cooling liquid. (See Zwischenbericht of May 6, 1936.)
(Items 1 and 4 are not included in report.)
1. Treatment of the cooling liquids of the paraffin oxidation carried out by Dr. Mannes and from the operation tests in Witten. Page 2.
2. Investigation of extraction gatsch. Page 14.
3. Investigation of the determination of the hydroxyl number of oxy acids according to the work of Dr. Hintermaier. Page 15.
4. Investigation of the determination of the ester number in paraffin acids. Page 16.
5. Tests on the de-hydroxylation of paraffin acids. Page 19.
6. Hydrogenation of paraffin oxidation products:
a. Oxides. Page 22
b. Acids. Page 26.
7. Chlorination of gatsch and conversion of the chlorination products. Page 31.
8. Treatment of whale oil according to the specifications of Dr. Ittner, Chief Chemist of Colgate, U.S.A. Page 32..
9. Preparation of p-n-dodecyl-cyclohexanol. Page 34.
1. Peroxides:
a. Percarbonates. Page 2.
b. Persulfate for the Schmidt distillation. Page 3.
c. Cooling liquid for plants. Page 7.
d. "Haftax" anodes. Page 9.
e. Preparation of per-salts according to Germ. Pat. Appl. S107939 of H. Schmidt. (One diagr. and graph attached.) Page 11.
2. Sodium silicate (water glass). "Krisit" crystallization. Page 12.
1. Peroxides:
a. Percarbonates. Page 2.
b. Persulfate electrolysis. Page 4.
c. Schmidt distillation. (Germ. Pat. Appl. S108,069.) Page 3.
d. Cooling liquid for plants. Page.
e. Perborate electrolysis. Page 8.
2. Water glass.
a. "Trax" colors. Page 9.
b. Metal silicate. Page 9.
1. Peroxides:
a. Percarbonates. (One graph attached.) Page 2.
b. Schmidt distillation. (Germ. Pat. Appl. Sch 107,364.) Page 5.
c. "Haftax" anodes. Page 9.
2. Sugar reduction. Page 9.
1. Peroxides:
a. Percarbonates. Page 2.
b. Schmidt distillation. Page 6.
c. Obtaining peroxides over azo compounds. Page 6.
2. Sugar reduction. Page 6.
1. Persulfate electrolysis:
a. Diaphragms. Page 1
b. Schmidt electrolyzer. Page.1.
c. Diaphragm electrode according to Schmidt, Germ. Pat. Appl. Sch 114,710. (One diagr. attached.) Page 2.
d. Electrolyte measurement. (One graph attached.) Page 2.
2. Percarbonates. Page 4.
3. Perborates:
a. Determination of heat of crystallization. Page 5.
b. Perborate preparation process. Page 5
4. Working up of used nickel catalyst. Page 7.
5. Electrolytic soap-splitting. Page 8.
1. Operation tests in Section 45/6. Page 1.
2. Laboratory experiment:
a. Purification of electrolytes. Page 2.
b. Electrolysis with Schmidt electrolytes. Page 4.
c. Diaphragm tests. Page 6.
d. Substitute material for "Koroseal." Page 9.
1. Persulfate electrolysis:
a. Diaphragms--"Spül" cathode according to Schmidt. Page 1.
b. Schmidt installation in Section 45/6. Page 1.
2. Percarbonates:
a. Improvement of stability. Page 2.
b. Preparation of percarbonates according to DEGUSSA. Page 6.
3. Electrolytic soap-splitting. (See Special Report of April 4, 1939.) Page 6. (Item 3 not included in report.)
1. Boron minerals. Page 1.
2. Percarbonates (electrolytic preparation):
a. Operation tests in Section 45/7. Page 2.
b. Laboratory tests. (One graph, two tables included.) Page 2.
3. Persulfate electrolysis:
a. Diaphragm cell according to Schmidt. (One graph included). Page 7.
b. Diaphragm tests. (Four photos included.) Page 8.
4. Electrolytic purification. Page 9.
5. Change of "Omag" into triphosphate. (See report of Sept. 29, 1939.) Page 11.
1. Change of pyro into ortho phosphate:
a. Laboratory tests for the "Omag" hydrolysis. Page 1.
b. Operation tests in the "Omag" oven of Section 53. Page 1.
2. Percarbonate preparation:
a. From barium peroxide. Page 2.
b. From Na2O2. Page 3.
3. Diaphragms for persulfate electrolysis. Page 7.
4. Schmidt installation in Section 45/6. Page 8.
5. Sodium silicate (water glass):
a. "Krisit" investigations for Section 50. Page 8.
b. Solubility of solid water glass in water. Page 8.
c. Water glass for camouflage. (See notice of Dec. 29, 1939.) Page 9.
1. Percarbonates:
a. Laboratory tests. (one large table included) Page 1.
b. Operation tests in Section 45/7. (One large table and one graph included.) Page 8.
2. Persulfate electrolysis:
a. Diaphragm tests. Page 12.
b. Acid purification. Page 14.
c. Schmidt installation. Page 14.
3. Boric acid. Page 15.
4. Whitewashing. Page 15.
5. Water glass filtration. Page 15.
6. Patent objections. Page 16.
1. Percarbonates:
a. Operation tests. Page 2.
b. DEGUSSA process. Page 2.
2. Persulfates--electrolysis, diaphragms. Page 3.
3. Hydrogen peroxide formation H2 and O2 gas mixtures by electrical discharge. Page 4.
a. Concentration of H2O2 solutions. Page 3.
b. Hydrogen peroxide formation from H2 and O2 gas mixtures by electrical discharge. Page 4.
4. Borax purification. Page 5.
5. Water glass section. Page 6.
6. Sodium chlorite. Page 7.
7. Sulfate waste water from the paraffin oxidation. Page.
8. Preparation of emulsions from fatty acid distillation residues. Page 8.
9. Patents. Page 11.
1. Hydrogen peroxide:
a. Distillation tests for the Schmidt installation.
b. Diaphragm tests for the Schmidt installation.
2. Water glass:
a. Treatment of sand with caustic soda.
b. Sodium silicate with alkali excess.
c. Egg conservation.
d. Water glass as dye binder.
e. Phosphate--alkali mixture.
f. Sodium sulfate from Witten for water glass.
g. Oven gas investigation by heating with UV (Unsaponifiable) Mersol.
h. Work planned.
3. Phosphate treatment according to the thermal process.
4. Sodium chlorite.
5. Potentiometric work.
6. Patents.
1. Working up of Witten soap glue:
a. Extraction with perchloro-ethylene:
1) Course of the extraction without alcohol addition.
2) Course of the extraction with aoxohol addition.
3) Foam formation in distillation of the soap solvents.
4) Driving off the perchloro-ethylene.
5) Differences in the working up of old and fresh soap.
6) Results of the extraction tests.
7) Classification of the U.V. (unsaponifiable) values of the perchloro-ethylene extraction tests.
b. Extractions with trichloro-ethylene:
1) Explosion phenomena in the working up of fatty acid--trichloro-ethylene mixtures.
2) Extractions with 1,5 vol. parts trichloro-ethylene.
3) Extractions with 2 vol. parts trichloro-ethylene.
4) Classification of the U.V. (unsaponifiable values of the trichloro-ethylene extraction tests.
c. Extractions with benzol and with benzene
2. Tests on the preparation of isopropenyl-glycol ether:
a. Action of ethylene oxide on acetone under pressure.
b. Action of ethylene oxide without pressure.
c. Result of these tests.
3. Conversion of melamine with acid chlorides:
a. Preparation of tristearyl melamine.
b. Preparation of trilauryl melamine.
c. Preparation of tricapronyl melamine.
4. Preparation of C-sulfo acids.
1. Continuous fat-splitting.
2. Feeding pigs with fat from first-run fatty acids.
3. Preparation of synthetic fats.
4. Deacidifying fish oil by esterification.
5. Various preparations.
6. Patent examples for the use of amido sulfonic acid.
(One diagram and several tables included in report.)
1. Separation of saturated and unsaturated compounds. (See report of Feb. 21, 1939.)
2. Process for the preparation of fatty acid esters. (See report of March 21, 1939.)
3. Investigation of the synthetic fats of M.S.J. (See report of March 24, 1939.)
4. Tests on continuous fat-splitting according to German Pat. Appl. 657,938. Second report.
5. Feeding pigs with fats from first-run fatty acids. Third report.
(One diagram and two tables are included with report. The first three items mentioned do not appear.)
1. Continuous fat-splitting according to German Pat. Appl. 657,938.
2. Synthetic fats:
a. Fatty acid purification.
b. Fat refining.
c. Testing of fats.
3. Process for the elimination of impurities from fats and process for the fractionation of fatty acids.
(See special report of May 17, 1939.) (Several tables and graphs included in report. Last item does not appear.)
1. Synthetic fats and their physiological valuation. (See special report of Feb. 8, 1940.)
2. Review of the synthetic fats prepared during Jan.-March 1940.
3. Process for the elimination of impurities from fats and process for the fractionation of fatty acids. III. (See report of March 12, 1940.)
4. Tests on the preparation of acid chlorides.
(Several tables included in report. Items 1 and 3 do not appear.)
1. The OXO synthesis:
a. Conversion of olefins with synthesis gas at various temperatures.
b. Synthesis with crack paraffins.
c. Synthesis with unsaturated alcohols.
d. Synthesis with unsaturated acids.
e. Synthesis with unsaturated aldehydes.
f. Synthesis with unsaturated ketones.
g. Synthesis with cyclic olefins.
2. Tests on the preparation of carboxylic acid chlorides from paraffins.
1. Separation of the water-soluble lower fatty acids. (See report of Sept. 25, 1940.)
2. Synthetic fats:
a. Preparation of new fats.
b. Tests on increasing the storagability and improving the odor of synthetic fats.
3. Addition of carbon monoxide and hydrogen to olefins:
a. Preparation of alcohols.
b. Conversion of crack olefins.
c. Addition of synthesis gas to "Puls-Pacura" crack distillate. (See report of Sept. 26, 1940.)
(Several tables included in report Item 1 and part c of item 3 do not appear.)
1. The production of synthetic fats.
2. The OXO synthesis:
a. The separation of olefins-paraffins.
b. The separation of alcohols--paraffins.
3. The OXO synthesis with olefins from Mersol.
4. The OXO synthesis with olefins from unsaponifiable Mersol.
120. Notes for the fixation of the paraffin oxidation process, signed by Dr. Lange, dated May 25, 1937, Section 51. Frames 2718-2720. 3 pp. This report is missing from the scanned images.
122. Apparatus for process described in Item 121. February 10, 1940. Frames 2727-2732. 8 pages.