Chapter 14 of 37 · 1533 words · ~8 min read

CHAPTER VIII

CHLOROPICRIN

During the spring of 1917, strange reports came from the Italian front that the Germans were using a new war gas. This gas, while it did not seem to be very poisonous, had the combined property of being a lachrymator and also of causing vomiting. Large number of casualties resulted through the men being forced to remove their masks in an atmosphere filled with lethal gases. The gas had the additional and serious disadvantage of being a very difficult one to remove completely in the gas mask. The first American masks were very good when chlorine or phosgene was considered but were of no value when chloropicrin was used.

One of the interesting facts of chemical warfare is that few if any new substances were discovered and utilized during the three years of this form of fighting. Chlorine and phosgene were well known compounds. And likewise, chloropicrin was an old friend of the organic chemist. So much so, indeed, that several organic laboratories prepared the compound in their elementary courses.

Chloropicrin was first prepared by the English chemist, Stenhouse, in 1848, by the action of bleaching powder upon a solution of picric acid. This was followed by a careful study of its physical and chemical properties, few of which have any connection with its use as a poison gas. The use of picric acid as an explosive made it very desirable that other raw materials should be used. Chloroform, which is the ideal source theoretically (since chloropicrin is nitro-chloroform, Cl₃CNO₂), gave very poor yields. While it may be prepared from acetone, in fair yields, acetone was about as valuable during the war as was picric acid. Practically all the chloropicrin used was prepared from this acid as the raw material.

MANUFACTURE

In the manufacture of chloropicrin the laboratory method was adopted. This consisted simply in passing live steam through a mixture of picric acid and bleaching powder. The resulting chloropicrin passes out of the still with the steam. There was a question at first whether a steam jacketed reaction vessel should be used, and whether stirrers should be introduced. Both types were tested, of which the simpler form, without steam jacket or stirrer, proved the more efficient.

[Illustration: FIG. 27.—Interior of Chloropicrin Plant.]

The early work was undertaken at the plant of the American Synthetic Color Company at Stamford, Connecticut. Later a large plant was constructed at Edgewood Arsenal. At the latter place ten stills, 8 by 18 feet, were erected, together with the necessary accessory equipment. The following method of operation was used:

The bleach is mixed with water and stirred until a cream is formed. This cream is then pumped into the still along with a solution of calcium picrate (picric acid neutralized with lime). When the current of live steam is admitted at the bottom of the still, the temperature gradually rises, until at 85° C. the reaction begins. The chloropicrin passes over with the steam and is condensed. Upon standing, the chloropicrin settles out, and may be drawn off and is then ready for filling into the shell. The yield was about 1.6 times the weight of picric acid used.

PROPERTIES

Chloropicrin is a colorless oil, which is insoluble in water, and which can be removed from the reaction by distillation with steam. It boils at 112° C. and will solidify at -69° C. At room temperature it has a density of 1.69 and is thus higher than chloroform (1.5) or carbon tetrachloride (1.59). At room temperature it has a vapor pressure of 24 mm. of mercury. It thus lies, in persistency, between such gases as phosgene on the one hand, and mustard gas on the other, but so much closer to phosgene that it is placed in the phosgene group.

Chloropicrin is a very stable compound and is not decomposed by water, acids or dilute alkalies. The reaction with potassium or sodium sulfite, in which all the chlorine is found as potassium or sodium chloride, has been used as an analytical method for its quantitative determination. The qualitative test usually used consists in passing the gas-air mixture through a heated quartz tube, which liberates free chlorine. The chlorine may be detected by passing through a potassium iodide solution containing starch, or by the use of a heated copper wire gauze, when the characteristic green color is obtained.

An interesting physiological test has also been developed. The eye has been found to be very sensitive to chloropicrin. The gas affects the eye in such a way that its closing is practically involuntary. A measurable time elapses between the instant of exposure and the time when the eye closes. Below 1 or 2 parts per million, the average eye withstands the gas without being closed, though considerable blinking may be caused. Above 25 parts, the reaction is so rapid as to render proper timing out of the question. But with concentrations between 2 and 25 parts, the subject will have an overpowering impulse to close his eye within 3 to 30 seconds. The time may be recorded by a stop watch and from the values thus determined a calibration curve may be plotted, using the concentration in parts per million and the time to zero eye reaction. Typical figures are given below. It will be noted that different individuals will vary in their sensitivity, though the order is the same.

+--------+---------+---------+ | Conc. | A | B | | p.p.m. | Seconds | Seconds | +--------+---------+---------+ | 20.0 | 4.0 | 5.0 | | 15.0 | 5.4 | 5.4 | | 10.0 | 7.5 | 7.5 | | 7.5 | 9.0 | 10.0 | | 5.0 | 13.0 | 15.0 | | 2.5 | 18.0 | 30.0 | +--------+---------+---------+

[Illustration: FIG. 28.—Calibration Curve of Eyes for Chloropicrin.]

PROTECTION

Because of the stability of chloropicrin, the question of protection resolves itself into finding an absorbent which is very efficient in removing the gas from air mixtures. Fortunately such an agent was found in the activated charcoal used in the American gas mask. The removal of the gas appears to take place in two stages. In the first, the gas is adsorbed in such a way that the long-continued passage of air does not remove it. In the second, the gas is absorbed, and this, really excess gas, is removed by pure air passing over the charcoal. The relation of these two factors has an important bearing on the quality of charcoal to be used in gas masks. It appears that up to a certain point an increase of the quality is desirable: beyond this, it is of doubtful value.

Unlike phosgene, chloropicrin is absorbed equally well at all temperatures. Moisture on the other hand has a very decided effect. It appears that charcoal absorbs roughly equivalent weights of chloropicrin and of water; the presence of water in the charcoal thus displaces an approximately equal amount of chloropicrin.

In the study of canisters it has been found that the efficiency time is approximately inversely proportional to the concentration. Formulas have been calculated to express the relation existing between concentration and life of the canister, and also between the rate of flow of the gas and the life.

While water seems to have a decidedly marked effect upon the life of a canister, this is not true of other gases, and the efficiency of the canister for each gas is not decreased when used in a binary mixture.

TACTICAL USES

Because of the high boiling point of chloropicrin it can only be used in shell. The German shell usually contained a mixture of superpalite (trichloromethyl chloroformate) and chloropicrin, the relative proportions being about 75 to 25. These were called Green Cross Shell, from the peculiar marking on the outside of the shell. Mixtures of phosgene and chloropicrin (50-50) have also been used.

The Allies have used a mixture of 80 per cent chloropicrin and 20 per cent stannic chloride (so-called N. C.). This mixture combines the advantages of a gas shell with those of a smoke shell, since the percentage of stannic chloride is sufficiently high to form a very good cloud. In addition to this, it is believed that the presence of the chloride increases the rate of evaporation of the chloropicrin. It has been claimed that the chloride decreases the amount of decomposition of the chloropicrin upon the bursting of the shell, but careful experiments appear to show that this decomposition is negligible and that the stannic chloride plays no part in it. This mixture was being abandoned at the close of the war.

This N. C. mixture has also been used in Liven’s projectors and in hand grenades. The material is particularly fitted for hand grenades, owing to the low vapor pressure of the chloropicrin, and the consequent absence of pressures even on warm days. As a matter of fact, it was the only filling used for this purpose, though later the stannic chloride was changed, owing to the shortage of tin, to a mixture of silicon and titanium chlorides.

While chloropicrin is sufficiently volatile to keep the strata of air above it thoroughly poisonous, it is still persistent enough to be dangerous after five or six hours.

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