| Wt. of boat | 2.6950 | 2.6950 |
| Wt. of boat and substance | 2.8470 | 2.8495 |
| Wt. of substance | .1520 | .1545 |
| KOH bulb | 50.9620 | 51.0805 |
| Bulb and CO2 | 51.3370 | 51.4610 |
| Wt. of CO2 | .3750 | .3805 |
| Carbon equivalent | .1023 | .10376 |
| Sulphuric acid tube | 76.2448 | 76.3450 |
| Tube and water | 76.3400 | 76.4453 |
| Wt. of water | .0952 | .1003 |
| Hydrogen equiv. | .0106 | .01114 |
| Percent Carbon | 67.3% | 67.2% |
| Percent hydrogen | 7.0% | 7.2% |
| Percent Oxygen | 25.7% | 25.6% |
An analysis of the iron salt obtained by precipitation from the potassium soap gave the following data.
| Wt. of substance used | .2955 | .3387 |
| Wt. of FeSO4 | .0445 | .0509 |
| Ferric equiv. | .03208 | .03676 |
| Percent Iron | 10.85% | 10.85% |
The following method was used in making the above analysis. The weighed material was ignited in a platinum crucible by gently heating until the combustible gases formed were given off. The crucible was then strongly heated until the carbonaceous material was completely burned off. The residue was weighed and the percentage of iron determined.
Expressed as the ACID NUMBER, or the number of milligrams of KOH required to neutralize the free acids in one gram of the substance, the following data was obtained.
| Ferric equivalent | .03208 | .03676 |
| Fe expressed as KOH equiv. | .0965 | .1107 |
| Wt. of material used | .2955 | .3387 |
| Mg. of KOH per gram | 326.6 | 326.7 |
| Acid number | 326.6 | 326.7 |
The following gives the ACID NUMBER obtained by direct titration of the Iron acid. The method is the same as that used in getting the titration value of the Barium acid.
| Wt. of substance | .2450 | .2472 |
| Cc of alkalie | 2.2 | 2.3 |
| KOH equiv. | .01232 | .01288 |
| KOH equiv. per gram | 53.87 | 52. |
An attempt was made to saponify some of the iron acid, but it was impossible. The alcohol was partially distilled off, and the acid freed by making the mass acid with sulphuric acid, and shaking out with ether. The ether was distilled off, but the remaining acid had different physical properties from the acid with which the experiment was started. It was lighter in color, and solidified at zero degrees. At room temperature it was almost solid. On ignition it left no ash. This probably is a polymerization product of the original acid.
Since many organic acids whose salts cannot be prepared by the ordinary methods can be prepared by passing dry ammonia gas through a solution of the acid in anhydrous ether, this method was tried with the iron acid. The iron acid was dissolved in anhydrous ether, and the dry ammonia gas was bubbled through this ether solution. At first no change was noted, but after several minutes there was a flocculent thready precipitate formed which was light brown in color. The experiment was repeated. At first the precipitate was a very light brown, but after forming it quickly darkened. After standing a few hours the flocculent precipitate changed to a sticky brown mass. This same change was produced immediately if the precipitate was exposed to the air. The resulting mass had no odor of ammonia.