But it has been asserted that while a large percentage (practically all) of the deaf can, by a great amount of painstaking and practice, become speech readers in some small degree, a relative degree of facility in articulation is not nearly so attainable. As to the accuracy of this view, the writer cannot venture an opinion. Judging from the average congenital deaf-mute who has had special instruction in speech, it can safely be asserted that their speech is laborious, and far, very far, from being accurate enough for practical use beyond a limited number of common expressions. This being the case, it is not surprising that as an unaided means of instruction it cannot be a success, for English neither understood when spoken, nor spoken by the pupil, cannot but remain a foreign language, requiring to pass through some other form of translation before it becomes intelligible.

There are the same obstacles in the use of the written or printed word as have been mentioned in connection with dactylology, namely, lack of rapidity in conveying impressions through the medium of the English sentence.

I have thus hastily reviewed the several means which teachers generally are employing to impart the use of English to deaf pupils, for the purpose of showing a common difficulty. The many virtues of each have been left unnoticed, as of no pertinence to this article.

The device suggested at the beginning of this paper, claiming to be nothing more than a school room appliance intended to supplement the existing means for giving a knowledge and practice of English to the deaf, employs as its interpreter a different sense from the one universally used. The sense of sight is the sole dependence of the deaf child. Signs, dactylology, speech reading, and the written and printed word are all dependent upon the eye for their value as educational instruments. It is evident that of the two senses, sight and touch, if but one could be employed, the choice of sight as the one best adapted for the greatest number of purposes is an intelligent one; but, as the choice is not limited, the question arises whether, in recognizing the superior adaptability to our purpose of the one, we do not lose sight of a possibly important, though secondary, function in the other. If sight were all-sufficient, there would be no need of a combination. But it cannot be maintained that such is the case. The plan by which we acquire our vernacular is of divine, and not of human, origin, and the senses designed for special purposes are not interchangeable without loss. The theory that the loss of a certain sense is nearly, if not quite, compensated for by increased acuteness of the remaining ones has been exploded. Such a theory accuses, in substance, the Maker of creating something needless, and is repugnant to the conceptions we have of the Supreme Being. When one sense is absent, the remaining senses, in order to equalize the loss, have imposed upon them an unusual amount of activity, from which arises skill and dexterity, and by which the loss of the other sense is in some measure alleviated, but not supplied. No additional power is given to the eye after the loss of the sense of hearing other than it might have acquired with the same amount of practice while both faculties were active. The fact, however, that the senses, in performing their proper functions, are not overtaxed, and are therefore, in cases of emergency, capable of being extended so as to perform, in various degrees, additional service, is one of the wise providences of God, and to this fact is due the possibility of whatever of success is attained in the work of educating the deaf, as well as the blind.

In the case of the blind, the sense of touch is called into increased activity by the absence of the lost sense; while in the case of the deaf, sight is asked to do this additional service. A blind person's education is received principally through the two senses of hearing and touch. Neither of these faculties is so sensible to fatigue by excessive use as is the sense of sight, and yet the eye has, in every system of instruction applied to the deaf, been the sole medium. In no case known to the writer, excepting in the celebrated case of Laura Bridgman and a few others laboring under the double affliction of deafness and blindness, has the sense of touch been employed as a means of instruction.[1]

[Footnote 1: This article was written before Professor Bell had made his interesting experiments with his "parents' class" of a touch alphabet, to be used upon the pupil's shoulder in connection with the oral teaching.--E.A.F.]

Not taking into account the large percentage of myopes among the deaf, we believe there are other cogent reasons why, if found practicable, the use of the sense of touch may become an important element in our eclectic system of teaching. We should reckon it of considerable importance if it were ascertained that a portion of the same work now performed by the eye could be accomplished equally as well through feeling, thereby relieving the eye of some of its onerous duties.

We see no good reason why such accomplishment may not be wrought. If, perchance, it were discovered that a certain portion could be performed in a more efficient manner, its value would thus be further enhanced.

In theory and practice, the teacher of language to the deaf, by whatever method, endeavors to present to the eye of the child as many completed sentences as are nominally addressed to the ear--having them "caught" by the eye and reproduced with as frequent recurrence as is ordinarily done by the child of normal faculties.

In our hasty review of the methods now in use we noted the inability to approximate this desirable process as a common difficulty. The facility now ordinarily attained in the manipulation of the type writer, and the speed said to have been reached by Professor Bell and a private pupil of his by the Dalgarno touch alphabet, when we consider the possibility of a less complex mechanism in the one case and a more systematic grouping of the alphabet in the other, would lead us to expect a more rapid means of communication than is ordinarily acquired by dactylology, speech (by the deaf), or writing. Then the ability to receive the communication rapidly by the sense of feeling will be far greater. No part of the body except the point of the tongue is as sensible to touch as the tips of the fingers and the palm of the hand. Tactile discrimination is so acute as to be able to interpret to the brain significant impressions produced in very rapid succession. Added to this advantage is the greater one of the absence of any more serious attendant physical or nervous strain than is present when the utterances of speech fall upon the tympanum of the ear. To sum up, then, the advantages of the device we find--

First. A more rapid means of communication with the deaf by syntactic language, admitting of a greater amount of practice similar to that received through the ear by normal children.

Second. Ability to receive this rapid communication for a longer duration and without ocular strain.

Third. Perfect freedom of the eye to watch the expression on the countenance of the sender.

Fourth. In articulation and speech-reading instruction, the power to assist a class without distracting the attention of the eye from the vocal organs of the teacher.

Fifth. Freedom of the right hand of the pupil to make instantaneous reproduction in writing of the matter being received through the sense of feeling, thereby opening the way for a valuable class exercise.

Sixth. The possible mental stimulus that accompanies the mastery of a new language, and the consequent ability to receive known ideas through a new medium.

Seventh. A fresh variety of class exercises made possible.

The writer firmly believes in the good that exists in all methods that are, or are to be; in the interdependence rather than the independence of all methods; and in all school-room appliances tending to supplement or expedite the labors of the teacher, whether they are made of materials delved from the earth or snatched from the clouds.

S. TEFFT WALKER,

Superintendent of the Kansas Institution, Olathe, Kans.


WATER GAS.

THE RELATIVE VALUE OF WATER GAS AND OTHER GASES AS IRON REDUCING AGENTS.

By B.H. THWAITE.

In order to approximately ascertain the relative reducing action of water gas, carbon monoxide, and superheated steam on iron ore, the author decided to have carried out the following experiments, which were conducted by Mr. Carl J. Sandahl, of Stockholm, who also carried out the analyses. The ore used was from Bilbao, and known as the Ruby Mine, and was a good average hematite. The carbonaceous material was the Trimsaran South Wales anthracite, and contained about 90 per cent. of carbon.

A small experimental furnace was constructed of the form shown by illustration, about 4 ft. 6 in. high and 2 ft. 3 in. wide at the base, and gradually swelling to 2 ft. 9 in. at the top, built entirely of fireclay bricks. Two refractory tubes, 2 in. square internally, and the height of the furnace, were used for the double purpose of producing the gas and reducing the ore.

The end of the lower tube rested on a fireclay ladle nozzle, and was properly jointed with fireclay; through this nozzle the steam or air was supplied to the inside of the refractory tubes. In each experiment the ore and fuel were raised to the temperature "of from 1,800 to 2,200 deg. Fahr." by means of an external fire of anthracite. Great care was taken to prevent the contact of the solid carbonaceous fuel with the ore. In each experiment in which steam was used, the latter was supplied at a temperature equivalent to 35 lb. to the square inch.

The air for producing the carbon monoxide (CO) gas was used at the temperature of the atmosphere. As near as possible, the same conditions were obtained in each experiment, and the equivalent weight of air was sent through the carbon to generate the same weight of CO as that generated when steam was used for the production of water gas.

First Experiment, Steam (per se).--Both tubes, A and B, were filled with ore broken to the size of nuts. The tube, A, was heated to about 2,000 deg. Fahr., the upper one to about 1,500 deg.

NOTE.--In this experiment, part of the steam was dissociated in passing through the turned-up end of the steam supply pipe, which became very hot, and the steam would form with the iron the magnetic oxide (Fe3O4). The reduction would doubtless be due to this dissociation. The pieces of ore found on lowest end of the tube, A, were dark colored and semi-fused; part of one of these pieces was crushed fine, and tested; see column I. The remainder of these black pieces was mixed with the rest of the ore contained in tube, A, and ground and tested; see column II. The ore in upper tube was all broken up together and tested; see column III. When finely crushed, the color of No. I. was bluish black; No. II., a shade darker red; No. III., a little darker than the natural color of the ore. The analyses gave:

-----------------------------+---------+---------+---------
                             |    I.   |   II.   |  III.
                             +---------+---------+---------
                             |per cent.|per cent.|per cent.
Ferric oxide (Fe_{2}O_{3}).  |  68.55  |  76.47  |  84.81
Ferrous oxide (FeO).         |  16.20  |   9.50  |   1.50
                             +---------+---------+---------
        Total.               |  84.75  |  85.97  |  86.31
                             +---------+---------+---------
Calculated:                  |         |         |
Ferric oxide (Fe_{2}O_{3}).  |  32.55  |  55.36  |  81.47
Magnetic oxide (Fe_{3}O_{4}).|  52.20  |  30.61  |   4.84
Ferrous oxide (FeO).         |         |         |
                             +---------+---------+---------
Total.                       |  84.75  |  85.97  |  86.31
                             +---------+---------+---------
Percentage of total
        oxygen reduced.      |   6.93  |   4.02  |   1.07
Metallic iron.               |  60.59  |  60.92  |  60.54
-----------------------------+---------+---------+---------

Second Experiment, Water Gas.--The tube, A, was filled with small pieces of anthracite, and heated until all the volatile matter had been expelled. The tube, B, was then placed in tube, A, the joint being made with fireclay, and to prevent the steam from carrying small particles of solid carbon into ore in the upper tube, the anthracite was divided from the ore by means of a piece of fine wire gauze. The steam at a pressure of about 35 lb. to the square inch was passed through the anthracite. The tube, A, was heated to white heat, the tube, B, at its lower end to bright red, the top to cherry red.

------------------+-----+-----+-----+-----+-----+-----+-----+-----+-----+-----+
Experiment.       |      1st.       |          2d.          |       3d.       |
------------------+-----+-----+-----+-----+-----+-----+-----+-----+-----+-----+
Number.           |  I. | II. | III.|  I. | II. | III.| IV. |  I. | II. | III.|
------------------+-----+-----+-----+-----+-----+-----+-----+-----+-----+-----+
Total Iron.       |60.59|60.92|60.54|65.24|61.71|61.93|57.23|59.73|57.93|55.54|
------------------+-----+-----+-----+-----+-----+-----+-----+-----+-----+-----+

Iron occurring as
------------------+-----+-----+-----+-----+-----+-----+-----+-----+-----+-----+
  FeO.            |12.60| 7.39| 1.17|46.98|18.59| 4.03| 0.84|29.45| 2.69| 1.12
  Fe_{2}O_{3}     |47.99|53.33|59.37|18.26|43.12|57.90|56.39|30.28|55.24|54.42
------------------+-----+-----+-----+-----+-----+-----+-----+-----+-----+-----+

Per cent. of Oxides.                                                          |
------------------+-----+-----+-----+-----+-----+-----+-----+-----+-----+-----+
  FeO.            |16.20| 9.50| 1.50|60.40|23.90| 5.18| 1.08|37.86| 3.46| 1.44
  Fe_{2}O_{3}.    |68.55|76.47|84.81|26.08|61.60|82.71|80.55|43.26|78.91|77.74
  Total.          |84.75|85.97|86.31|86.48|85.50|87.89|81.63|81.12|82.37|79.18
------------------+-----+-----+-----+-----+-----+-----+-----+-----+-----+-----+

Oxygen in Ore.
------------------+-----+-----+-----+-----+-----+-----+-----+-----+-----+-----+
Before experiment.|25.97|26.10|26.05|27.96|26.45|26.54|24.52|25.60|24.81|23.80
After experiment. |24.16|25.05|25.77|21.24|23.79|25.96|24.40|21.39|24.44|23.64
  Difference.     | 1.81| 1.05| 0.28| 6.72| 2.66| 0.58| 0.12| 4.21| 0.37| 0.16
------------------+-----+-----+-----+-----+-----+-----+-----+-----+-----+-----+

Per cent. of oxygen reduced.
------------------+-----+-----+-----+-----+-----+-----+-----+-----+-----+-----+
  oxygen reduced. | 6.93| 4.02| 1.07|24.03|10.02| 2.18| 0.49|16.44| 1.49| 0.42
------------------+-----+-----+-----+-----+-----+-----+-----+-----+-----+-----+

Degree of Oxidation of the Ore after the Experiment.
------------------+-----+-----+-----+-----+-----+-----+-----+-----+-----+-----+
FeO.              | ... | ... | ... |84.66| ... | ... | ... |18.40| ... | ... |
Fe_{3}O_{4}.      |52.20|30.61| 4.84|37.82|77.01|28.12| 3.88|62.72|11.14| 4.64|
Fe_{2}O_{3}.      |32.55|55.36|81.47| ... | 8.49|59.77|77.75| ... |71.23|74.54|
Total.            |84.75|85.97|85.97|85.97|85.97|85.97|85.97|85.97|85.97|85.97|
------------------+-----+-----+-----+-----+-----+-----+-----+-----+-----+-----+

------------------+-----------------+-----------------------+-----------------+
The ore having    |                 |                       |                 |
been exposed to   |     Steam.      |     Water gas.        | Carbon monoxide.|
------------------+-----------------+-----------------------+-----------------+

Four Samples were Tested.--I. The bottom layer, 1¼ in. thick; the color of ore quite black, with small particles of reduced spongy metallic iron. II. Layer above I., 4¼ in. thick; the color was also black, but showed a little purple tint. III. Layer above II., 5 in. thick; purple red color. IV. Layer above III., ore a red color. The analyses gave:

-----------------------------+---------+---------+---------+---------
                             |    I.   |   II.   |  III.   |   IV.
                             +---------+---------+---------+---------
                             |per cent.|per cent.|per cent.|per cent.
Ferric oxide (Fe_{2}O_{3}).  |  26.08  |  61.60  |  82.71  |  80.55
Ferrous oxide (FeO).         |  60.40  |  23.90  |   5.18  |   1.08
                             +---------+---------+---------+---------
        Total.               |  86.48  |  85.50  |  87.89  |  81.63
                             +---------+---------+---------+---------
Calculated:                  |         |         |         |
Ferric oxide (Fe_{2}O_{3}).  |   ...   |   8.49  |  59.77  |  77.75
Magnetic oxide (Fe_{3}O_{4}).|  37.82  |  77.01  |  28.12  |   3.88
Ferrous oxide (FeO).         |  48.66  |         |         |
                             +---------+---------+---------+---------
Total.                       |  86.48  |  85.41  |  87.89  |  81.63
                             +---------+---------+---------+---------
Percentage of total
        oxygen reduced.      |  24.03  |  10.02  |   2.26  |   0.49
Metallic iron.               |  65.24  |  61.71  |  61.93  |  57.23
-----------------------------+---------+---------+---------+---------

NOTE.--All the carbon dioxide (CO2) occurring in the ore as calcic carbonate was expelled.

Third Experiment, Carbon monoxide (CO).--The tube A was filled with anthracite in the manner described for the second experiment, and heated to drive off the volatile matter, before the ore was placed in the upper tube, B, and the anthracite was divided from the ore by means of a piece of fine wire gauze. The lower tube, A, was heated to the temperature of white heat, the upper one, B, to a temperature of bright red. I. Layer, 1 in. thick from the bottom; ore dark brownish colored. II. Layer 4 in. thick above I.; ore reddish brown. III. Layer 11 in. thick above II.; ore red color. The analyses gave:

-----------------------------+---------+---------+---------
                             |    I.   |   II.   |  III.
                             +---------+---------+---------
                             |per cent.|per cent.|per cent.
Ferric oxide (Fe_{2}O_{3}).  |  43.26  |  78.91  |  77.74
Ferrous oxide (FeO).         |  37.86  |   3.46  |   1.44
                             +---------+---------+---------
        Total.               |  81.12  |  82.37  |  79.18
                             +---------+---------+---------
Calculated:                  |         |         |
Ferric oxide (Fe_{2}O_{3}).  |   ...   |  71.23  |  74.54
Magnetic oxide (Fe_{3}O_{4}).|  62.72  |  11.14  |   4.64
Ferrous oxide (FeO).         |  18.40  |         |
                             +---------+---------+---------
Total.                       |  81.12  |  82.37  |  79.18
                             +---------+---------+---------
Percentage of total
        oxygen reduced.      |  16.44  |   1.49  |   0.42
Metallic iron.               |  59.73  |  57.93  |  55.54
-----------------------------+---------+---------+---------

NOTE.--The carbon monoxide (CO) had failed to remove from the ore the carbon dioxide existing as calcic carbonate. The summary of experiments in the following table appears to show that the water gas is a more powerful reducing agent than CO in proportion to the ratio of as

                 4.21 x 100
4.21 : 6.72, or ------------ = 52 per cent.
                      72

Mr. B.D. Healey, Assoc. M. Inst. C.E., and the author are just now constructing large experimental plant in which water gas will be used as the reducing agent. This plant would have been at work before this but for some defects in the valvular arrangements, which will be entirely removed in the new modifications of the plant.


ANTISEPTIC MOUTH WASH.

Where an antiseptic mouth wash is needed, Mr. Sewill prescribes the use of perchloride of mercury in the following form: One grain of the perchloride and 1 grain of chloride of ammonium to be dissolved in 1 oz. of eau de Cologne or tincture of lemons, and a teaspoonful of the solution to be mixed with two-thirds of a wineglassful of water, making a proportion of about 1 of perchloride in 5,000 parts.--Chemist and Druggist.


ANNATTO.

[Footnote: Read at an evening meeting of the North British Branch of the Pharmaceutical Society, January 21.]

By WILLIAM LAWSON.

The subject which I have the honor to bring shortly before your notice this evening is one that formed the basis of some instructive remarks by Dr. Redwood in November, 1855, and also of a paper by Dr. Hassall, read before the Society in London in January, 1856, which latter gave rise to an animated discussion. The work detailed below was well in hand when Mr. MacEwan drew my attention to these and kindly supplied me with the volume containing reports of them. Unfortunately, they deal principally with the adulterations, while I was more particularly desirous to learn the composition in a general way, and especially the percentage of coloring resin, the important constituent in commercial annatto. Within the last few years it was one of the articles in considerable demand in this part of the country; now it is seldom inquired for. This, certainly, is not because butter coloring has ceased to be employed, and hence the reason for regretting that the percentage of resin was not dealt with in the articles referred to, so that a comparison could have been made between the commercial annatto of that period and that which exists now. In case some may not be in possession of literature bearing on it--which, by the way, is very meager--it may not be out of place to quote some short details as to its source, the processes for obtaining it, the composition of the raw material, and then the method followed in the present inquiry will be given, together with the results of the examination of ten samples; and though the subject doubtless has more interest for the country than for the town druggist, still, I trust it will have points of interest for both.

Annatto is the coloring matter derived from the seeds of an evergreen plant, Bixa Orellana, which grows in the East and West Indian Islands and South America, in the latter of which it is principally prepared. Two kinds are imported, Spanish annatto, made in Brazil, and flag or French, made mostly in Cayenne. These differ considerably in characters and properties, the latter having a disagreeable putrescent odor, while the Spanish is rather agreeable when fresh and good. It is, however, inferior to the flag as a coloring or dyeing agent. The seeds from which the substance is obtained are red on the outside, and two methods are followed in order to obtain it. One is to rub or wash off the coloring matter with water, allow it to subside, and to expose it to spontaneous evaporation till it acquires a pasty consistence. The other is to bruise the seeds, mix them with water, and allow fermentation to set in, during which the coloring matter collects at the bottom, from which it is subsequently removed and brought to the proper consistence by spontaneous evaporation. These particulars, culled from Dr. Redwood's remarks, may suffice to show its source and the methods for obtaining it.

Dr. John gives the following as the composition of the pulp surrounding the seeds: Coloring resinous matter, 28; vegetable gluten, 26.5; ligneous fiber, 20; coloring, 20; extractive matter, 4; and a trace of spicy and acid matter.

It must be understood, however, that commercial annatto, having undergone processes necessary to fit it for its various uses, as well as to preserve it, differs considerably from this; and though it may not be true, as some hint, that manufacturing in this industry is simply a term synonymous with adulterating, yet results will afterward be given tending to show that there are articles in the market which have little real claim to the title. I tried, but failed, to procure a sample of raw material on which to work, with a view to learn something of its characters and properties in this state, and thus be able to contrast it with the manufactured or commercial article. The best thing to do in the circumstances, I thought, was to operate on the highest priced sample at disposal, and this was done in all the different ways that suggested themselves. The extraction of the resin by means of alcohol--the usual way, I believe--was a more troublesome operation than it appeared to be, as the following experiment will show: One hundred grains of No. 8 were taken, dried thoroughly, reduced to fine powder, and introduced into a flask containing 4 ounces of alcohol in the form of methylated spirit, boiled for an hour--the flask during the operation being attached to an inverted condenser--filtered off, and the residue treated with a smaller amount of the spirit and boiled for ten minutes. This was repeated with diminishing quantities until in all 14 ounces had been used before the alcoholic solution ceased to turn blue on the addition to it of strong sulphuric acid, or failed to give a brownish precipitate with stannous chloride. As the sample contained a considerable quantity of potassium carbonate, in which the resin is soluble, it was thought that by neutralizing this it might render the resin more easy of extraction. This was found to be so, but it was accompanied by such a mass of extractive as made it in the long run more troublesome, and hence it was abandoned. Thinking the spirit employed might be too weak, an experiment with commercial absolute alcohol was carried out as follows: One hundred grains of a red sample, No. 4, were thoroughly dried, powdered finely, and boiled in 2 ounces of the alcohol, filtered, and the residue treated with half an ounce more. This required to be repeated with fresh half ounces of the alcohol until in all 7½ were used; the time occupied from first to last being almost three hours. This was considered unsatisfactory, besides being very expensive, and so it, also, was set aside, and a series of experiments with methylated spirit alone was set in hand. The results showed that the easiest and most satisfactory way was to take 100 grains (this amount being preferred, as it reduces error to the minimum), dry thoroughly, powder finely, and macerate with frequent agitation for twenty-four hours in a few ounces of spirit, then to boil in this spirit for a short time, filter, and repeat the boiling with a fresh ounce or so; this, as a rule, sufficing to completely exhaust it of its resin. Wynter Blyth says that the red resin, or bixin, is soluble in 25 parts of hot alcohol. It appears from these experiments that much more is required to dissolve it out of commercial annatto.

The full process followed consisted in determining the moisture by drying 100 grains at 212° F. till constant, and taking this dried portion for estimation of the resin in the way just stated. The alcoholic extract was evaporated to dryness over a water-bath, the residue dissolved in solution of sodium carbonate, and the resin precipitated by dilute sulphuric acid (these reagents being chosen as the best after numerous trials with others), added in the slightest possible excess. The resin was collected on a tared double filter paper, washed with distilled water until the washings were entirely colorless, dried and weighed.

The ash was found in the usual way, and the extractive by the difference. In the ash the amount soluble was determined, and qualitatively examined, as was the insoluble portion in most of them.

The results are as follows:

         |  1.  |  2.  |  3.  |  4.  |  5.  |  6.  |  7.  |  8.  |  9.  |  10.
Moisture | 21.75| 21.60| 20.39| 69.73| 18.00| 18.28| 15.71| 38.18| 19.33| 22.50
Resin    |  3.00|  2.90|  1.00|  8.80|  3.00|  1.80|  5.40| 12.00|  5.90|  9.20
Extrac-
tive     | 57.29| 59.33| 65.00| 19.47| 58.40| 65.67| 26.89| 20.82| 23.77| 28.50
Ash      | 17.96| 16.17| 13.61|  2.00| 20.60| 14.25| 52.00| 29.00| 51.00| 39.80
-------------------------------------------------------------------------------
         |100.00|100.00|100.00|100.00|100.00|100.00|100.00|100.00|100.00|100.00
-------------------------------------------------------------------------------
Ashes:   |      |      |      |Almost|      |      |      |      |      |
Soluble  | 13.20| 12.57|  7.50|wholly|  10.0| 11.75| 18.5 | 20.0 | 15.0 | 13.8
Insoluble|  4.76|  3.60|  6.11| NaCl.|  10.6|  2.50| 33.5 |  9.0 | 36.0 | 26.0

The first six are the ordinary red rolls, with the exception of No. 4, which is a red mass, the only one of this class direct from the manufacturers. The remainder are brown cakes, all except No. 7 being from the manufacturers direct. The ash of the first two was largely common salt; that of No. 3 contained, besides this, iron in some quantity. No. 4 is unique in many respects. It was of a bright red color, and possessed a not disagreeable odor. It contained the largest percentage of moisture and the lowest of ash; had, comparatively, a large amount of coloring matter; was one of the cheapest, and in the course of some dairy trials, carried out by an intelligent farmer, was pronounced to be the best suited for coloring butter. So far as my experience goes, it was a sample of the best commercial excellence, though I fear the mass of water present and the absence of preserving substances will assist in its speedy decay. Were such an article easily procured in the usual way of business, there would not be much to complain of, but it must not be forgotten that it was got direct from the manufacturers--a somewhat suggestive fact when the composition of some other samples is taken into account. No. 5 emitted a disagreeable odor during ignition. The soluble portion of the ash was mostly common salt, and the insoluble contained three of sand--the highest amount found, although most of the reds contained some. No. 6 was a vile-looking thing, and when associated in one's mind with butter gave rise to disagreeable reflections. It was wrapped in a paper saturated with a strongly smelling linseed oil. When it was boiled in water and broken up, hairs, among other things, were observed floating about. It contained some iron. The first cake, No. 7, gave off during ignition an agreeable odor resembling some of the finer tobaccos, and this is characteristic more or less of all the cakes. The ash weighed 52 per cent., the soluble part of which, 18.5, was mostly potassium carbonate, with some chlorides and sulphates; the insoluble, mostly chalk with iron and alumina. No. 8--highest priced of all--had in the mass an odor which I can compare to nothing else than a well rotted farmyard manure. Twenty parts of the ash were soluble and largely potassium carbonate, the insoluble being iron for the most part. The mineral portions of Nos. 9 and 10 closely resemble No. 7.

On looking over the results, it is found that the red rolls contained starchy matters in abundance (in No. 4 the starch was to a large extent replaced by water), and an ash, mostly sodium chloride, introduced no doubt to assist in its preservation as well as to increase the color of the resin--a well known action of salt on vegetable reds. The cakes, which are mostly used for cheese coloring, I believe, all appeared to contain turmeric, for they gave a more or less distinct reaction with the boric acid test, and all except No. 8 contained large quantities of chalk. These results in reference to extractive, etc., reveal nothing that has not been known before. Wynter Blyth, who gives the only analyses of annatto I have been able to find, states that the composition of a fair commercial sample (which I take to mean the raw article) examined by him was as follows: water, 24.2; resin, 28.8; ash, 22.5; and extractive, 24.5; and that of an adulterated (which I take to mean a manufactured) article, water, 13.4; resin, 11.0; ash (iron, silica, chalk, alumina, and common salt), 48.3; and extractive. 27.3. If this be correct, it appears that the articles at present in the market, or at least those which have come in my way, have been wretched imitations of the genuine thing, and should, instead of being called adulterated annatto, be called something else adulterated, but not seriously, with annatto. I have it on the authority of the farmer previously referred to, that ¼ of an ounce of No. 4 is amply sufficient to impart the desired cowslip tint to no less than 60 lb. of butter. When so little is actually required, it does not seem of very serious importance whether the adulterant or preservative be flour, chalk, or water, but it is exasperating in a very high degree to have such compounds as Nos. 3 and 6 palmed off as decent things when even Nos. 1, 2, and 5 have been rejected by dairymen as useless for the purpose. In conclusion, I may be permitted to express the hope that others may be induced to examine the annatto taken into stock more closely than I was taught to do, and had been in the habit of doing, namely, to see if it had a good consistence and an odor resembling black sugar, for if so, the quality was above suspicion.


JAPANESE RICE WINE AND SOJA SAUCE.

Professor P. Cohn has recently described the mode in which he has manufactured the Japanese sake or rice wine in the laboratory. The material used was "Tane Kosi," i.e., grains of rice coated with the mycelium, conidiophores, and greenish yellow chains of conidia of Aspergillus Oryzoe. The fermentation is caused by the mycelium of this fungus before the development of the fructification. The rice is first exposed to moist air so as to change the starch into paste, and then mixed with grains of the "Tane Kosi." The whole mass of rice becomes in a short time permeated by the soft white shining mycelium, which imparts to it the odor of apple or pine-apple. To prevent the production of the fructification, freshly moistened rice is constantly added for two or three days, and then subjected to alcoholic fermentation from the Saccharomyces, which is always present in the rice, but which has nothing to do with the Aspergillus. The fermentation is completed in two or three weeks, and the golden yellow, sherry-like sake is poured off. The sample manufactured contained 13.9 per cent. of alcohol. Chemical investigation showed that the Aspergillus mycelium transforms the starch into glucose, and thus plays the part of a diastase.

Another substance produced from the Aspergillus rice is the soja sauce. The soja leaves, which contain little starch, but a great deal of oil and casein, are boiled, mixed with roasted barley, and then with the greenish yellow conidia powder of the Aspergillus. After the mycelium has fructified, the mass is treated with a solution of sodium chloride, which kills the Aspergillus, another fungus, of the nature of a Chalaza, and similar to that produced in the fermentation of "sauerkraut," appearing in its place. The dark-brown soja sauce then separates.


ALUMINUM.

[Footnote: Annual address delivered by President J.A. Price before the meeting of the Scranton Board of Trade, Monday, January 18, 1886.]

By J.A. PRICE.

Iron is the basis of our civilization. Its supremacy and power it is impossible to overestimate; it enters every avenue of development, and it may be set down as the prime factor in the world's progress. Its utility and its universality are hand in hand, whether in the magnificent iron steamship of the ocean, the network of iron rail upon land, the electric gossamer of the air, or in the most insignificant articles of building, of clothing, and of convenience. Without it, we should have miserably failed to reach our present exalted station, and the earth would scarcely maintain its present population; it is indeed the substance of substances. It is the Archimedean lever by which the great human world has been raised. Should it for a moment forget its cunning and lose its power, earthquake shocks or the wreck of matter could not be more disastrous. However axiomatic may be everything that can be said of this wonderful metal, it is undoubtedly certain that it must give way to a metal that has still greater proportions and vaster possibilities. Strange and startling as may seem the assertion, yet I believe it nevertheless to be true that we are approaching the period, if not already standing upon the threshold of the day, when this magical element will be radically supplanted, and when this valuable mineral will be as completely superseded as the stone of the aborigines. With all its apparent potency, it has its evident weaknesses; moisture is everywhere at war with it, gases and temperature destroy its fiber and its life, continued blows or motion crystallize and rob it of its strength, and acids will devour it in a night. If it be possible to eliminate all, or even one or more, of these qualities of weakness in any metal, still preserving both quantity and quality, that metal will be the metal of the future.

The coming metal, then, to which our reference is made is aluminum, the most abundant metal in the earth's crust. Of all substances, oxygen is the most abundant, constituting about one-half; after oxygen comes silicon, constituting about one-fourth, with aluminum third in all the list of substances of the composition. Leaving out of consideration the constituents of the earth's center, whether they be molten or gaseous, more or less dense as the case may be, as we approach it, and confining ourselves to the only practical phase of the subject, the crust, we find that aluminum is beyond question the most abundant and the most useful of all metallic substances.

It is the metallic base of mica, feldspar, slate, and clay. Professor Dana says: "Nearly all the rocks except limestones and many sandstones are literally ore-beds of the metal aluminum." It appears in the gem, assuming a blue in the sapphire, green in the emerald, yellow in the topaz, red in the ruby, brown in the emery, and so on to the white, gray, blue, and black of the slates and clays. It has been dubbed "clay metal" and "silver made from clay;" also when mixed with any considerable quantity of carbon becoming a grayish or bluish black "alum slate."

This metal in color is white and next in luster to silver. It has never been found in a pure state, but is known to exist in combination with nearly two hundred different minerals. Corundum and pure emery are ores that are very rich in aluminum, containing about fifty-four per cent. The specific gravity is but two and one-half times that of water; it is lighter than glass or as light as chalk, being only one-third the weight of iron and one-fourth the weight of silver; it is as malleable as gold, tenacious as iron, and harder than steel, being next the diamond. Thus it is capable of the widest variety of uses, being soft when ductility, fibrous when tenacity, and crystalline when hardness is required. Its variety of transformations is something wonderful. Meeting iron, or even iron at its best in the form of steel, in the same field, it easily vanquishes it at every point. It melts at 1,300 degrees F., or at least 600 degrees below the melting point of iron, and it neither oxidizes in the atmosphere nor tarnishes in contact with gases. The enumeration of the properties of aluminum is as enchanting as the scenes of a fairy tale.

Before proceeding further with this new wonder of science, which is already knocking at our doors, a brief sketch of its birth and development may be fittingly introduced. The celebrated French chemist Lavoisier, a very magician in the science, groping in the dark of the last century, evolved the chemical theory of combustion--the existence of a "highly respirable gas," oxygen, and the presence of metallic bases in earths and alkalies. With the latter subject we have only to do at the present moment. The metallic base was predicted, yet not identified. The French Revolution swept this genius from the earth in 1794, and darkness closed in upon the scene, until the light of Sir Humphry Davy's lamp in the early years of the present century again struck upon the metallic base of certain earths, but the reflection was so feeble that the great secret was never revealed. Then a little later the Swedish Berzelius and the Danish Oersted, confident in the prediction of Lavoisier and of Davy, went in search of the mysterious stranger with the aggressive electric current, but as yet to no purpose. It was reserved to the distinguished German Wohler, in 1827, to complete the work of the past fifty years of struggle and finally produce the minute white globule of the pure metal from a mixture of the chloride of aluminum and sodium, and at last the secret is revealed--the first step was taken. It took twenty years of labor to revolve the mere discovery into the production of the aluminum bead in 1846, and yet with this first step, this new wonder remained a foetus undeveloped in the womb of the laboratory for years to come.

Returning again to France some time during the years between 1854 and 1858, and under the patronage of the Emperor Napoleon III., we behold Deville at last forcing Nature to yield and give up this precious quality as a manufactured product. Rose, of Berlin, and Gerhard, in England, pressing hard upon the heels of the Frenchman, make permanent the new product in the market at thirty-two dollars per pound. The despair of three-quarters of a century of toilsome pursuit has been broken, and the future of the metal has been established.

The art of obtaining the metal since the period under consideration has progressed steadily by one process after another, constantly increasing in powers of productivity and reducing the cost. These arts are intensely interesting to the student, but must be denied more than a reference at this time. The price of the metal may be said to have come within the reach of the manufacturing arts already.

A present glance at the uses and possibilities of this wonderful metal, its application and its varying quality, may not be out of place. Its alloys are very numerous and always satisfactory; with iron, producing a comparative rust proof; with copper, the beautiful golden bronze, and so on, embracing the entire list of articles of usefulness as well as works of art, jewelry, and scientific instruments.

Its capacity to resist oxidation or rust fits it most eminently for all household and cooking utensils, while its color transforms the dark visaged, disagreeable array of pots, pans, and kitchen implements into things of comparative beauty. As a metal it surpasses copper, brass, and tin in being tasteless and odorless, besides being stronger than either.

It has, as we have seen, bulk without weight, and consequently may be available in construction of furniture and house fittings, as well in the multitudinous requirements of architecture. The building art will experience a rapid and radical change when this material enters as a component material, for there will be possibilities such as are now undreamed of in the erection of homes, public buildings, memorial structures, etc. etc., for in this metal we have the strength, durability, and the color to give all the variety that genius may dictate.

And when we take a still further survey of the vast field that is opening before us, we find in the strength without size a most desirable assistant in all the avenues of locomotion. It is the ideal metal for railway traffic, for carriages and wagons. The steamships of the ocean of equal size will double their cargo and increase the speed of the present greyhounds of the sea, making six days from shore to shore seem indeed an old time calculation and accomplishment. A thinner as well as a lighter plate; a smaller as well as a stronger engine; a larger as well as a less hazardous propeller; and a natural condition of resistance to the action of the elements; will make travel by water a forcible rival to the speed attained upon land, and bring all the distant countries in contact with our civilization, to the profit of all. This metal is destined to annihilate space even beyond the dream of philosopher or poet.

The tensile strength of this material is something equally wonderful, when wire drawn reaches as high as 128,000 pounds, and under other conditions reaches nearly if not quite 100,000 pounds to the square inch. The requirements of the British and German governments in the best wrought steel guns reach only a standard of 70,000 pounds to the square inch. Bridges may be constructed that shall be lighter than wooden ones and of greater strength than wrought steel and entirely free from corrosion. The time is not distant when the modern wonder of the Brooklyn span will seem a toy.

It may also be noted that this metal affords wide development in plumbing material, in piping, and will render possible the almost indefinite extension of the coming feature of communication and exchange--the pneumatic tube.

The resistance to corrosion evidently fits this metal for railway sleepers to take the place of the decaying wooden ties. In this metal the sleeper may be made as soft and yielding as lead, while the rail may be harder and tougher than steel, thus at once forming the necessary cushion and the avoidance of jar and noise, at the same time contributing to additional security in virtue of a stronger rail.

In conductivity this metal is only exceeded by copper, having many times that of iron. Thus in telegraphy there are renewed prospects in the supplanting of the galvanized iron wire--lightness, strength, and durability. When applied to the generation of steam, this material will enable us to carry higher pressure at a reduced cost and increased safety, as this will be accomplished by the thinner plate, the greater conductivity of heat, and the better fiber.

It is said that some of its alloys are without a rival as an anti-friction metal, and having hardness and toughness, fits it remarkably for bearings and journals. Herein a vast possibility in the mechanic art lies dormant--the size of the machine may be reduced, the speed and the power increased, realizing the conception of two things better done than one before. It is one of man's creative acts.

From other of its alloys, knives, axes, swords, and all cutting implements may receive and hold an edge not surpassed by the best tempered steel. Hulot, director in the postage stamp department, Paris, asserts that 120,000 blows will exhaust the usefulness of the cushion of the stamp machine, and this number of blows is given in a day; and that when a cushion of aluminum bronze was substituted, it was unaffected after months of use.

If we have found a metal that possesses both tensile strength and resistance to compression; malleability and ductility--the quality of hardening, softening, and toughening by tempering; adaptability to casting, rolling, or forging; susceptibility to luster and finish; of complete homogeneous character and unusually resistant to destructive agents--mankind will certainly leave the present accomplishments as belonging to an effete past, and, as it were, start anew in a career of greater prospects.

This important material is to be found largely in nearly all the rocks, or as Prof. Dana has said, "Nearly all rocks are ore-beds of the metal." It is in every clay bank. It is particularly abundant in the coal measures and is incidental to the shales or slates and clays that underlie the coal. This under clay of the coal stratum was in all probability the soil out of which grew the vegetation of the coal deposits. It is a compound of aluminum and other matter, and, when mixed with carbon and transformed by the processes of geologic action, it becomes the shale rock which we know and which we discard as worthless slate. And it is barely possible that we have been and are still carting to the refuse pile an article more valuable than the so greatly lauded coal waste or the merchantable coal itself. We have seen that the best alumina ore contains only fifty-four per cent. of metal.

The following prepared table has been furnished by the courtesy and kindness of Mr. Alex. H. Sherred, of Scranton.