Fig. I THE AERO-STEAM DISINFECTOR.Fig. I
Fig. II THE AERO-STEAM DISINFECTOR.Fig. IITHE AERO-STEAM DISINFECTOR.
The disinfecting apparatus, illustrated in a portable and stationary form, of the dimensions adopted by the sanitary authorities of Vienna, Budapest, Prague, Lemberg, Teplitz, etc., and by the Imperial and Royal Theresianum Institute, and sanctioned for use in barracks, military hospitals, etc., by the Austrian Ministry of War, and for ambulance hospitals by the Red Cross, acts by means of a mixture of steam and hot air in such proportion that the steam, after expending its mechanical energy in inducting the hot air into the disinfecting chamber, is, by contact with the clothes or bedding of a lower temperature, not only condensed, but by condensation completely neutralizes the risk of injury through any chance excess of hot air. The boiler being practically open is inexplosive, and requires neither safety valves nor skilled attendance.
The heat generated in the furnace is utilized to the utmost, and the escaping vapors form a steam jacket in the double casing of the disinfecting chamber. The method of manipulation reduces the danger of contagion to a minimum, as the clothes or bedding are placed in specially constructed sacks in the sick chamber itself, and, after being tightly closed, the sacks are removed and hung in the disinfector. The stationary apparatus, which is constructed to disinfect four complete suits of clothes, including underlinen, or one complete set of bedding, including mattress, is specially adapted for hospitals, barracks, jails, etc. Its dimensions can easily be increased, but the size shown has proved itself, from an economical point of view, the best, as, where the quantity of articles to be disinfected varies, several apparatus can be erected at a less cost than one large one, and one or more be heated as the quantity of infected articles be small or large. In the accompanying drawing A is the boiler, which is filled by pouring water into the reservoir, B, until the same, entering the boiler at its lowest part through the tube, C, rises to the desired height in the water gauge, G. C acts also in the place of a safety valve. D is the fire space, E a movable grate, and F the coal hopper. The fuel consists of charcoal or coke. The boiler is emptied by the cock, H. I is a steam pipe connecting the steam space with the hot air tube, L¹. K is an auxiliary pipe to admit the steam into the chimney during stoppage for emptying and recharging the disinfecting chamber in continuous working. The admission of air is regulated by the handle, L, and the draught in the chimney, M, by the handle, N. O is the disinfecting chamber inclosed by the space, P, which acts at the same time as a steam jacket and as a channel for the downward passage of the vapors escaping from the chamber through the outlets, S. The lower portion of the disinfecting chamber, Q, is funnel-shaped for the better mixture and distribution of the steam and hot air, and to collect any condensation water. Q¹ is a sieve to catch any fallen article. The vertical tubes, S, which serve at the same time to strengthen the chamber, connect the lower portion of the steam jacket, P, with the circular channel, T, which is again connected with the chimney, M, by the tube, T'. The disinfection chamber is hermetically closed by the double cover, R, to the lower plate of which hooks for hanging the sacks are fastened. The cover fits in a sand bath, and is raised and lowered by means of the pulley chain, W, and the swinging crane, X. U is a thermometer indicating the temperature of the steam and hot air in the disinfecting chamber, V a cock for drawing off any condensation water, Y a battery connected with an electrical thermometer to be placed in the clothes or bedding, and Z the sacks in which the infected articles are hung.
The portable apparatus, as shown, for heating with gas, or even spirits of wine, can also be heated with a similar steam and hot air apparatus as the stationary disinfector. In country towns or villages, or even in cities, whose architectural arrangements permit, the portable disinfector can easily be drawn by one man into the courtyard or garden of any house, and the process of disinfection conducted on the spot. Its usefulness in campaigns for ambulance hospitals is self-evident. The letters denoting the several parts are the same as in the stationary apparatus. The portable disinfector is constructed to disinfect two complete suits of clothes or one mattress. The extremely favorable results are shown in the accompanying table of trials.—The Engineer.
TABLE OF RESULTS WITH WM. E. THURSFIELD'S STEAM AND HOT AIR DISINFECTORS.
Series of Trials.I.II.III.IV.V.VI.VII.VIII.IX.X.XI.XII.XIII.XIV.XV.Portable Apparatus.Stationary Apparatus.Contents of boiler, ingallons3.854.18—4.184.184.185.75.710.010.010.010.010.010.010.0Water added during the process—1.54————1.40.64.3——7.41.4——Temperature of waterdegs. Fah.———725754431325446176434343104Firing commenced with spirits of wine athours min.—2.129.104.30—10.0—————————Firing commenced with gas athours min.1.30———3.0——————————Firing commenced with coke athours min.———————1.10—8.151.131.432.54——Firing commenced with charcoal athours min.——————10.12—2.15————8.4310.16Steam generated athours min.—2.349.284.413.1510.1810.351.342.388.531.202.33.199.310.23212 deg. in chamber registered by external thermometer athours min.2.302.409.34———10.501.522.459.31.282.183.379.1210.31212 deg. in clothes registered by electrical thermometer athours min.———5.254.1812.12————1.55————221 deg. in clothes registered by electrical thermometer athours min.——————11.512.34———3.504.2610.412.03Highest temperature in chamber registered by external thermometerdeg.—270250—324255302275293320284284302284275Mean temperature in chamber registered by external thermometerdeg.241257239266—253266266284284266266284266266Trial closed athours, min.4.454.1011.45.454.3012.3011.512.354.3011.02.103.504.3510.1012.03Max. therm. registered in mattressdeg.262——————————————Max. therm. registered in overcoatdeg.—239226———223223253244226———223Max. therm. registered in winter coatdeg.———232223214—————230232223—Max. therm. regis'd in winter trousersdeg.—243239—————262—253————Max. therm. regis'd in summer trousersdeg.—246252—————280—264————Time required to generate steammin.—22181115182324233872025207Time required to generate 212 deg. in chambermin.602824———384230481535432915Time required to generate 212 deg. in clothesmin.———5578132————42————Time required to generate 221 deg. in clothesmin.——————9985———1279281107Total duration of processmin.135118114759015099851351055712710187107Water evaporated, ingallons———1.651.902.754.33.36.93——9.24—3.634.84Consumption of spirits of winepints———3.0—9.6—————————Consumption of gas, incubic feet————70——————————Consumption of cokes, incbs———————6——8.816.5———Consumption of charcoal, incbs——————8.8——————14.313.8
N.B.—In every case, even in the trials V. and X., in which the temperature in the disinfecting chamber rose above 320 deg. Fah., the clothes, owing to the complete saturation of the hot air with live steam, remained absolutely unimpaired.The column "water evaporated" shows the quantity of live steam passing through the disinfecting chamber averages 13 cubic feet per minute with gas or spirits, and 22 cubic feet with charcoal or coke in the portable and 33 cubic feet in the stationary apparatus. Trials VI., VII., and VIII. took place in open air.According to trial XII., from 28 to 30 complete suits of clothes can be disinfected at an expenditure of about 75 cbs. of coke per diem.
N.B.—In every case, even in the trials V. and X., in which the temperature in the disinfecting chamber rose above 320 deg. Fah., the clothes, owing to the complete saturation of the hot air with live steam, remained absolutely unimpaired.
The column "water evaporated" shows the quantity of live steam passing through the disinfecting chamber averages 13 cubic feet per minute with gas or spirits, and 22 cubic feet with charcoal or coke in the portable and 33 cubic feet in the stationary apparatus. Trials VI., VII., and VIII. took place in open air.
According to trial XII., from 28 to 30 complete suits of clothes can be disinfected at an expenditure of about 75 cbs. of coke per diem.
This arrangement consists in a cylindrical metal or horn mounted lens two to four centimeters long, and magnifying two or three times, and two or three centimeters in diameter, whose side is provided with a contrivance for holding after it has been pushed into place a copying needle, a protractor, etc.
While hitherto the architect in using millimeter paper must hold separately in his hands a magnifying glass and needle, while the engraver holds the engraving tool inclined in one hand and the magnifying glass in the other, or must work under a large lens standing on three feet, it is now possible by a firm connection between the lens and needle or other instrument to draw directly with one hand and under the lens. In the accompanying cut one of these lenses is shown in section, A, in which the glass is set obliquely, in whose focus the needle,a, is held and the field of view is enlarged. A longer description is unnecessary, as the illustration gives the best explanation. It need only be remarked that the stud,s, projecting a little near the glass, is for the purpose of preventing the instrument from leaving the position coinciding with the plane of the drawing. For architects and engineers is provided a small compass,b, of about 2 cm. diameter, for laying off parallel widths, for making smaller scales and the like. In these cases it is substituted for the needle. In like manner for calculating cross profiles by graphical methods, for reading parallel divisions, for estimating areas, or revising maps, a finely divided prismatic ivory rule,c, can be placed under the glass, B, and will do good service. In this case the plane of the lens must be perpendicular to the axis of the tube.
IMPROVED DRAWING INSTRUMENT.IMPROVED DRAWING INSTRUMENT.
For draughtsmen a parallel drawing pen, something likeb, is used, which gives several lines at once, perfectly parallel and close together; or a drawing pen with which the smallest signatures, such as boundary stones and figures, can be made neatly and exactly, which is secured like the needle,a, and for which the cylinder serves also as pen holder, offers a great advance.
Thus a whole series of instruments can be used with the lens. For instance, a naturalist can use with it a knife or other instrument. To avoid injury from the instruments, one should, in laying down the cylinder, place it on its side. It is also recommended that on the outer tube of the frame, which is appropriately lacquered of black color, white arrows should be placed in the direction of the points of the instrument, so that the eyes shall be protected from injury in handling the instrument, as by the points being stuck into the pupil, owing to lifting the instrument in an inverted position.—Zeitschrift fur Instrumentenkunde.
That style of machine for moulding candles in which the candles are forced out at the top by means of a piston is the one most employed, and it is an apparatus of this kind that we illustrate herewith. In its construction, this apparatus presents some important improvements in detail which it is of interest to set forth. The improvements made by the Messrs. Barlow have been studied with a view of manufacturing candles with conical ends, adapted to all chandeliers, without interfering with rapidity of production or increasing the net cost.
These gentlemen have likewise so simplified the continuous system of drawing the wick along as to prevent any loss of cotton. In the next place, the structure of the moulds, properly so called, is new. Instead of being cast, as is usually the case, they are rolled and drawn out, thus giving them smooth surfaces and permitting of their being soldered, are assembled by means of threaded bronze sockets. The engravings between Figs. 3 and 4 show these two modes of fixation. Atamay be seen the old method of junction by soldering, and atbthe screwing of the moulds into the socket. This machine consists of a box which is alternately heated and cooled, and which is fixed upon aframe, A, at the lower part of which are located the wick bobbins, E. Toward the top of the machine there is a mechanism for actuating the two pairs of jaws, B, which grasp the candles forced upward by the play of the pistons, D. This mechanism, which is controlled by a lever, acts by means of an eccentric.
Fig. 1Fig. 1Fig. 2. BARLOW'S CANDLE MOULDING MACHINE.Fig. 2.BARLOW'S CANDLE MOULDING MACHINE.
Fig. 1Fig. 1
Fig. 2. BARLOW'S CANDLE MOULDING MACHINE.Fig. 2.
BARLOW'S CANDLE MOULDING MACHINE.
The pistons, D, are hollow, and are provided above with pieces which form the small end of the candles. Instead of using tin, as is usually done, the Messrs. Barlow employ galvanized iron in the construction of these pistons, and mount them through screw rings—no soldering being used. For this reason, any workman whatever can quickly replace one of the tubes. All the pistons are placed upon a horizontal table, which is made to rise and descend at will, in order to regulate the length of the candles and remove them from the mould. A winch transmits the motion which is communicated to it to two pairs of pinions that gear with racks fixed to the frame to lift the table that supports the pistons. How these latter are mounted may be seen from an inspection of Figs. 3 to 5. This new arrangement of spiral springs for the purpose is designed to hold the pistons on the table firmly, and at the same time to prevent the shock that their upper ends might undergo in case of an abrupt turn of the winch. Moreover, the forged iron plate, H, is not exposed to breakage as it is in other machines, where it is of cast iron. The bobbins already mentioned revolve upon strong iron rods, and the moving forward of the wick in the moulds is effected automatically by the very fact of the manufactured candles' being forced out. These latter are held in position through the double play of the jaws, B, while the stearic acid is flowing into the upper part of the moulds. The cotton wick is thus drawn along and kept in the axis of the candles.
Figs. 1 and 2. BARLOW'S CANDLE MOULDING MACHINE.Figs. 3, 4, and 5.BARLOW'S CANDLE MOULDING MACHINE.
One peculiarity of the machine consists in the waste system applied to the mould box. Steam or hot or cold water is sent into the latter through the conduit, L, starting from a junction between pipes provided with cocks. When the water contained in the box is in excess, it flows out through the waste pipes, G, which terminate in a single conduit. Owing to the branchings at T, and to the cocks of the conduits that converge at L, it is very easy to vary the temperature of the box at will. The warm or cold water or steam may be admitted or shut off simultaneously.
When first beginning operations, the wick is introduced into each mould by hand. The piston table is raised by means of the winch, and is held in this position through the engaging of a click with a ratchet on the windlass. A fine iron rod long enough to reach beneath the pistons and catch the end of the wick is next introduced. After this is removed, the wick is fixed once for all, and in any way whatever, to the top of the mould. This operation having been accomplished, the piston table is lowered, and the machine is ready to receive the stearic acid. The moulds are of tin and are open at both ends. In order to facilitate the removal of the candles, they are made slightly conical. When the candles have hardened, the ends are equalized with a wooden or tin spatula, and then the piston table is raised. At this instant, the jaws, B, are closed so as to hold the candles in place. The latter, in rising, pull into the mould a new length of wick, well centered. A slight downward tension is exerted upon the wick by hand, then a new operation is begun. During this time, the candles held between the jaws having become hard, their wicks are now cut by means of the levers, C, and they are removed from the machine and submitted to a finishing process.—Revue Industrielle.
In several former notes and articles in these pages, we have spoken of the severe crisis through which the old established, or "Leblanc," process has now for some years been passing. It is, in fact, pushed well nigh out of the running by the newer process, known as the "ammonia-soda" process, and would have had to give up the battle before now were it not for the fact that one of its by-products, bleaching powder, cannot, so far, be produced at all by the ammonia-soda works. The bleaching powder trade has thus remained in the hands of the workers of the Leblanc process, and its sale has enabled them to cover much of the loss which they are suffering on the manufacture of soda ash and caustic soda.
In brief outline, the old Leblanc process consists in the following operations: Salt is decomposed and boiled down with sulphuric acid. Sulphate of sodium is formed, and a large amount of hydrochloric acid is given off. This is condensed, and is utilized in the manufacture of the bleaching powder mentioned above. The sulphate of sodium, known as "salt cake," is mixed with certain proportions of small coal and limestone, and subjected to a further treatment in a furnace, by which a set of reactions take place, causing the conversion of the sulphate of sodium of the "salt cake" into carbonate of sodium, a quantity of sulphide of calcium being produced at the same time. The mass resulting from this process is known as "black ash." It is extracted with water, which dissolves out the carbonate of sodium, which is sold as such or worked into "caustic" soda, as may be required. The insoluble residue is the "alkali waste," which forms the vast piles, so hideous to look at and so dreadful to smell, which surround our large alkali works.
The sulphuric acid required for the conversion of the salt into "salt cake" is made by the alkali manufacturer himself, this manufacture necessitating a large plant of "lead chambers" and accessories, and keeping up an immense trade in pyrites from Spain and Portugal. The development of the alkali trade in this country has been something colossal, and the interests involved in it and connected with it are so great that anything affecting it may safely be said to be of truly national importance, quite apart from what technical interest it may possess.
The "ammonia-soda" process, which has played such havoc with the old style of manufacture, proceeds on totally different lines. Briefly stated, it depends on the fact that if a solution of salt in water is mixed with bicarbonate of ammonium, under proper conditions, a reaction takes place by which the salt, or chloride of sodium, is converted at once into bicarbonate of sodium, the bicarbonate of ammonium being at the same time converted into chloride of ammonium.
The bicarbonate of sodium settles out at once as insoluble crystals, easily removed, marketable at once as such, or easily converted into simple carbonate of sodium, and further into caustic soda, as in the ordinary "old" process. The residual chloride of ammonium is decomposed by distillation with lime, giving ammonia for reconversion into bicarbonate of ammonium, and chloride of calcium, which is a waste product.
The maker of "ammonia" soda works direct on the brine, as pumped from the salt fields. His plant is simpler and less costly, and he arrives at his first marketable product much more rapidly and with very much lower working costs than the maker of Leblanc soda, in spite of all the great mechanical improvements which have of late years been introduced into the old process, and which have cheapened its work.
The original patents on the use of ammonium bicarbonate have, we understand, long since expired. But the working details of the process and much of the most successful apparatus have undergone great development and improvement during late years, all the important points being covered by patents still in force, and mainly, if not wholly, in the hands of the one large firm which is now carrying on the manufacture in this country, and is controlling the market.
The one weak spot of the ammonia-soda process, as we mentioned before, is its inability to supply hydrochloric acid or chlorine, and so allow of making bleaching powder. Time after time it has been announced positively that the problem was solved, that the ammonia-sodamakers had devised a method of producing hydrochloric acid or chlorine, or both, without the use of sulphuric acid. But the announcements have so far proved baseless, and at present the Leblanc makers are getting incredulous, and do not much excite themselves over new statements of the kind, though they know that if once their rivals had this weapon in their hands the battle would be over and the Leblanc process doomed to rapid extinction.
Such is at present the state of the struggle in this great industry, and the above outline sketch of the two processes is designed to give some idea of the conditions to such of our readers as may not have any special knowledge of these manufactures.
At the present moment great interest is being taken in a new process, about to be put to work on a large scale, which is designed to take up the cudgels against the ammonia process and enable the Leblanc makers to continue the fight on something more like equal terms.
We allude to the process proposed and patented by Messrs. Parnell & Simpson, and about to be worked by the "Lancashire Alkali and Sulphur Company," at Widnes. We recently had the opportunity of inspecting fully the plant erected, and of having the method of procedure explained to us. We look upon the new process as such a spirited attempt to turn the tide of a long and losing battle, and as so very interesting on its own merits, that an account of it in these pages will be thoroughly in place.
The main idea of the process is to combine the "Leblanc" and the "ammonia-soda" manufacture. But in place of using caustic lime to decompose the ammonium chloride and get back the ammonia, the "alkali waste" spoken of above is employed, it being found that not only is the ammonia driven off, but that also the sulphur in the "waste" is obtained in a form allowing of its easy utilization, it and the ammonia combining to form ammonium sulphide, which passes over in gaseous form from the decomposing apparatus. This ammonium sulphide is, as we shall see, quite as available for the working of the ammonia-soda manufacture as pure and simple ammonia, and all the sulphur can be obtained from it.
In outline the process is as follows: We will suppose that a quantity of bicarbonate of sodium has been just precipitated from a brine solution, and we have the residual ammonium chloride to deal with. This is decomposed by "alkali waste," giving a final liquor of calcium chloride, which is run to waste, and a quantity of ammonium sulphide gas. This latter is led at once into a solution of salt in water, till saturation takes place. Into this liquor of brine and ammonium sulphidepurecarbonic acid gas is now passed. The ammonium sulphide is decomposed, pure sulphureted hydrogen gas is given off, which is conducted to a gas holder and stored, while ammonium bicarbonate is formed in the liquor, which brings about the conversion of the salt into bicarbonate of sodium, ready for removal and preparation for the market.
It will be observed that we printed the wordpurein italics in speaking of the carbonic acid used. This is one of the great points in the process, as in order that the sulphureted hydrogen gas obtained shall be concentrated and pure, only pure carbonic acid can be used in liberating it. The apparatus employed in its preparation is perhaps the most ingenious part of the works, and well worthy of attention by others besides alkali makers. The method is based on the fact that if dilute impure carbonic acid is passed into a solution of carbonate of sodium, the carbonic acid is absorbed, bicarbonate of sodium being formed, and the diluting gases passing away.
The bicarbonate of sodium on heating gives up the extra carbonic acid, which can be collected and stored pure, while the liquor passes back to simple carbonate of sodium, to be used over again as an absorbent. This is not at all new in theory, of course, nor is this the first proposal to use it commercially; but it is claimed that this is the first successful working of it on a large scale.
The gases from a large limekiln supply the dilute carbonic acid gas, which contains 25 per cent. to 30 per cent. of pure gas, the principal diluting gas being, of course, nitrogen. This kiln gas is drawn from the kiln by a blowing engine, and is first cooled in two large receivers. It is then forced into the solution of sodium carbonate in the absorption tower, 65 ft. high by 6 ft. diameter, filled with the liquor. The tower has many diaphragms and perforated "mushrooms," to cause a proper dispersion of the gases as they ascend through the liquor. The strength of liquor found best adapted for the work is equal to a density of about 30° Twaddell. After saturation the mud of bicarbonate of sodium is drawn off and passed into the "decomposer," a tower 35 ft. high by 6 ft. 6 in. in diameter, with perforated shelves, into which steam is blown from below, the liquor passing downward. The bicarbonate is decomposed, pure carbonic acid being given off. This is passed through a scrubber and into a gas holder ready for use. The liquor, which has now returned to the state of simple carbonate of sodium, only requires cooling to be ready to absorb a fresh lot of carbonic acid gas. The cooling is effected in a tower packed loosely with bricks, the hot liquor trickling down against a powerful current of air blown in from below. Liquor has been cooled in this way, in once passing through the tower, from 220° Fahr. to 58° Fahr., but of course the exact cooling obtained depends more or less on the temperature of the atmosphere.
The next stage of the process, if we follow on after the preparation of the pure carbonic acid, is the employment of the gas for the decomposition of the ammonium sulphide absorbed in a brine liquor as above explained. The brine and ammonium sulphide are contained in what is known as a "Solvay tower," provided with proper means for dispersion and absorption of the carbonic acid gas. The precipitated bicarbonate of sodium is removed and washed, and prepared for the market in whatever form is required, the sulphureted hydrogen gas being led to a holder and stored, as before stated.
The decomposition of the ammonium chloride by means of "alkali waste" is carried out in a specially designed still. This is a tower 45 ft. high by 8 ft. diameter, divided by horizontal plates into compartments of about 3 ft. 8 in. in height. These compartments communicate with one another by means of pockets, or recesses, in the shell of the tower. A vertical shaft, with arms, revolves in the tower. The "waste" is fed in at the top by means of hopper and screw feed. The liquor is heated by steam blown in to over 212° Fahr. The ammonium sulphide is led direct into an absorbing vessel full of brine.
It now only remains to see how it is proposed to deal with the sulphureted hydrogen gas which represents the sulphur recovered from the waste. It can be burnt direct to sulphurous acid and utilized for the production of vitriol perfectly pure and free from arsenic, commanding a special price. But Messrs. Parnell & Simpson state that by a method of restricted combustion they are able to obtain nearly all the sulphur as such, and put it on the market on equal terms with the best Sicilian sulphur. We did not gather that this has yet been done on the working scale, however.
It will be seen that it is proposed that a Leblanc alkali maker shall continue to produce a portion of his make by the old process, but shall erect plant to enable him to make another portion by the Parnell & Simpson method, using his Leblanc "waste" in place of the caustic lime now employed by the ammonia soda people. He is thus to have the benefit of the cheaper process for, say, half his make, while he further cheapens the ammonia method by saving the cost of lime and by recovering the sulphur otherwise lost in his waste.
The saving in lime is stated to be one ton for each ton of sodium carbonate produced, or in cash value about 10s. per ton at Widnes, while the sulphur saved is estimated to be 6 cwt. per ton of sodium carbonate. We reproduce these figures with all reserve, not being ourselves sufficiently specialists to judge of them. But we were assured that they represent the minimum expected, and reasons were given to us to show that they would probably be exceeded.
Another gain for the Leblanc maker would be that he will escape the cost of removal and disposal of a portion of his refuse or waste.
The plant now erected was calculated for a yield of one hundred tons carbonate of sodium and about thirty-five tons of sulphur per week, but it now appears likely that this will be exceeded; while the carbonic acid plant was supposed to be equal to a yield of 6 tons of pure gas per day, and is now found capable of doing twice as much.
A few weeks will now bring this new combination process into the active and crucial test of the markets. Chemists and chemical engineers have all along taken a keen interest in the ingenious ideas of Parnell & Simpson. Commercial men are no less interested in the financial result of the experiment about to be tried at the expense of a few gentlemen of Liverpool and district. So far as we can learn, opinions are to some extent divided, though many good judges are very hopefully inclined. For our own part, speaking with diffidence, as being a little off our regular track of work, we will only say that we were favorably impressed with what we saw and heard; and we certainly wish the venture that full success which its cleverness and its pluck, as well as its great importance at this crisis, deserve for it.—Engineering.
An important subject for investigation, which has not yet been satisfactorily determined, is the temperature at which it is most beneficial to distill coals of various qualities. The practice of allowing the charge to remain in the retort for some time after most of the gas has been driven off, to enable (it is said) the retort to recover heat for the next charge, often leads to misconception as to the true temperature of carbonization. The effect of this is to equalize the temperatures inside and outside the retort. This inside temperature is not maintained, the temperature outside not being high enough to transmit the heat with sufficient rapidity; and so, in an apparently hot retort, the coal may be carbonized at a comparatively low temperature. A truer test of temperature is that of the outside of the retort, which should be not less than 400° to 500° Fahr. above the temperature necessary for proper carbonization. In all experiments relating to temperature pretending to any degree of accuracy, a pyrometer of some kind should be used. Judging of the temperature by the color is often misleading. Not only may the eye be deceived, but different clays do not present the same appearance at the same temperature. A good, reliable pyrometer to estimate temperatures to (say) 2500° Fahr. is much wanted.
Experience during the last few years with the high temperatures obtained by the use of regenerative furnaces has led me to the conclusion that higher heats than are usual may be employed with advantage, as regards both the quantity and the quality of gas, provided the retorts are heated uniformly throughout their length, and the weight and duration of the charge are so adjusted that the coal does not remain longer in the retort than is just sufficient to drive off the gas; and that the more rapidly the coal is carbonized, the better are the results. In two retorts of the same size, one making 5,000 and the other 10,000 cubic feet per day, the gas will be twice as long in contact with the surface of the retort in the former as in the latter—to the probable detriment of its quality, and increased tendency to stoppage in the ascension pipes.
A subject closely allied to that just alluded to is the temperature of the gas as it leaves the retort. Until within the last few years, it was generally assumed that this was not higher than from 200° to 300° Fahr.; and a very plausible theory was given to account for such a comparatively low temperature. A discussion which took place a few years ago in theJournal of Gas Lightingshowed that at that time opinions on this subject were not unanimous. But the conclusion arrived at seemed to be that the gas was not higher in temperature than that before stated; and if higher temperatures were observed, they were due to the tarry matter in the gas, and were not those of the gas itself. A little reflection is sufficient to show that the existence of gas intimately mixed with tarry matter at a high temperature, without being itself raised to that temperature, is a physical impossibility.
In a paper read to a Continental gas association about a year ago, the writer stated, as the result of many experiments, that unless the temperature in the ascension pipe rises above 480° Fahr., thickening of the tar in the hydraulic main and choking of the ascension pipe will certainly occur. This led me to make a series of experiments, extending over many months, on the temperature of the gas in the ascension pipes at different points and at various times during the charge. The results of these experiments may be of some interest, and may lead to further investigation. The temperatures were taken by mercurial thermometers registering 600° Fahr., except those near the mouthpiece, which were taken by a Siemens water pyrometer. Every care was exercised to insure accuracy; and the instruments were carefully adjusted. At a distance of 18 inches from the mouthpiece, the temperatures varied from an average of 890°, shortly after the retort was charged, to 518° at the end of the charge; at 12 feet distant from the mouthpiece, the corresponding temperature was 444°, falling to 167° at the end of the charge; and at 22 feet, the average temperature varied from 246° at the commencement to 144° at the end of the charge. These are the averages of a number of experiments. In some instances they were considerably above these averages—temperatures over 900° being frequently obtained. This is about the temperature of a low red heat, and is much higher than any I have seen recorded. When the gas was allowed to issue from a hole in the ascension pipe, 1¼ inches in diameter, 18 inches above the mouthpiece, a strip of lead held about an inch from the orifice was freely melted.
In the settings on which these experiments were made, the middle ascension pipe takes the gas from the two central retorts; and it is of interest to note that in this pipe the temperature of the gas 18 inches from the upper retort was found to be 1014° Fahr., and at the point where it entered the hydraulic main it was 440° Fahr. Zinc was freely melted by the gas issuing from a hole 18 inches from the mouthpiece. The temperatures always fall toward the end of the charge; the fall of temperature in the ascension pipe being a good indication that the charge is worked off. They increase with the heat of the retort and with the weight of the charge.
Experiments were also made to ascertain the temperature of the gas in the retort; and for this purpose one of Murrie's pyrometers was used, the action of which depends on the pressure produced by the vaporization of mercury in a malleable iron tube. The end of this tube was first rested on the top of the coal, but not in contact with the retort. It reached about 18 inches into the retort, and therefore was not in the hottest part. In this position the temperature indicated shortly after charging the retort was 1110° Fahr., gradually rising to 1640° Fahr. The end of the tube was then embedded in the coal, when the pyrometer indicated a temperature of 1260° Fahr. within 30 minutes after the retort was charged; gradually rising toward the end of the charge as before. At the time these temperatures were taken, the retorts were each producing 10,000 cubic feet of gas per day. I had no opportunity of testing the accuracy of the statement that, with lower temperatures, there is a tendency to stoppage of the ascension pipes; but with these high temperatures (contrary to what might be expected) there is no trouble from stoppages.
These experiments, so far as they have gone, lead to the conclusion that the temperature of the gas as it is evolved from the coal is not less than 1200° Fahr., and that cooling commences immediately on the gas leaving the retort. The temperatures being far above that of liquefaction, the gases are cooled very rapidly. The temperature of the gas in the ascension pipe depends on the rapidity with which the gas is evolved—that is to say, the greater the quantity produced in a given time, the less effective is the cooling action of the mouthpiece and the ascension pipe; and although I had no opportunity of testing it, I should expect to find that with retorts making from 5,000 to 6,000 cubic feet of gas per day, the maximum temperature in the ascension pipe 18 inches from the mouthpiece will not exceed 400° to 500° Fahr., while with lower heats and lighter charges the temperatures will be still lower. That these temperatures have some effect in causing or preventing stoppage in the ascension pipes there can be no doubt; and it is important that this subject should be thoroughly investigated.
It is of interest to consider what must be the physical condition of the gas at these high temperatures. All the hydrocarbons which are afterward condensed must then be in the condition of gases having various degrees of condensability, mixed with and rendered visible by a cloud of carbon particles or soot. If this soot could be removed from the gas at this stage without reducing the temperature, we should probably have no thick tar or pitch, but only comparatively light-colored oils; and it might possibly lead to an entirely different mode of conducting the process of condensation.
These are a few of the subjects on which it is extremely desirable that we should possess that complete information which can only be obtained by well-directed investigations with different materials and under varying conditions. There are many others in connection with carbonization and purification which might be mentioned; but I think I have said sufficient to show the necessity that exists for more minute investigation and research. Investigations such as are here indicated do not involve any large expenditure of money; but they do require care and intelligence to prevent errors being made. Experiments should not be condemned as defective because the results differ from old-established theories; yet when this does happen, it is in all cases better to suspect the new experiment rather than the old theory, until the results have been fully established.—Wm. Foulis, Journal of Gas Lighting.
The Widnes Alkali Company have recently erected an enormous revolving black ash furnace, which is 30 ft. in length and has a diameter of 12 ft. 6 in. The inside length is 28 ft. 6 in., with a diameter of 11 ft. 4 in. The furnace is lined with 16,000 fire bricks and 120 fire-clay breakers, each weighing 1¼ cwt. The weight of salt cake per charge,i.e., contained in each charge of salt cake, limestone, mud, and slack, is 8 tons 12 cwt. For 110 tons of salt cake charged there are also used about 100 tons of lime mud and limestone and 55 tons of mixing slack. The total amount of salt cake decomposed weekly is about 400 tons, which may be calculated to yield 240 tons of 60 per cent. caustic soda. There is claimed for this massive furnace an economy in iron plate, in expense on the engine power and on fuel consumed, as well as on wear and tear.—Watson Smith, in Industries.
The inauguration of the statue of Philip Lebon, the inventor of lighting by gas, occurred on the 26th of June, at Chaumont, under the auspices of the Technical Gas Society of France. The statue, which we illustrate herewith, is due to the practiced chisel of the young sculptor Antide Pechine, who has perfectly understood his work, and has represented the inventor at the moment at which he observes a flame start from a glass balloon in which he had heated some sawdust. The attitude is graceful and the expression of the face is meditative and intelligent. The statue, which is ten feet in height, was exhibited at the lastSalon. It was cast at the Barbedienne works.
It would be impossible to applaud too much the homage that has just been rendered to the inventor of gas lighting, for Philip Lebon, like so many other benefactors of humanity, has not by far the celebrity that ought to belong to him. When we study the documents that relate to his existence, when we follow the flashes of genius that darted through his brain, when we see the obstacles that he had to conquer, and when we thoroughly examine his great character and the lofty sentiments that animated him, we are seized with admiration for the humble worker who endowed his country with so great a benefit.
Lebon was born at Brachay on the 29th of May, 1767. At the age of twenty, he was admitted to the School of Bridges and Roads, where he soon distinguished himself by his ingenious and investigating turn of mind. His first labors were in connection with the steam engine, then in its infancy, and on April 18, 1792, the young engineer obtained a national award of $400 to continue the experiments that he had begun on the improvement of this apparatus.
It was at about the same epoch that Lebon was put upon the track of lighting by gas, during a sojourn at Brachay. He one day threw a handful of sawdust into a glass vial that he heated over a fire. He observed issuing from the bottle a dense smoke which suddenly caught fire and produced a beautiful luminous flame. The inventor understood the importance of the experiment that he had just performed, and resolved to work it further. He had just found that wood and other combustibles were, under the action of heat, capable of disengaging a gas fit for lighting and heating. He had seen that the gas which is disengaged from wood is accompanied with blackish vapors of an acrid and empyreumatic odor. In order that it might serve for the production of light, it was necessary to free it from these foreign products.
Lebon passed the vapor through a tube into a flask of water, which condensed the tarry and acid substances, and the gas escaped in a state of purity. This modest apparatus was the first image of the gas works; and it comprised the three essential parts thereof—the generating apparatus, the purifying apparatus, and the receiver for collecting the gas.
One year afterward, the inventor had seen Fourcroy, Prony, and the great scientists of his epoch. On the 28th of September, 1799, he took out a patent in which he gives a complete description of his thermo lamp, by means of which he produced a luminous gas, while at the same time manufacturing wood tar and pyroligneous or acetic acid. In this patent he mentions coal as proper to replace wood, and he explains his system with a visible emotion and singular ardor. In reading what he has written we are struck with that form of persuasion that does not permit of doubting that he foresaw the future in reserve for his system.
Unfortunately, Lebon could not devote all his time to his discovery. Being a government engineer, without money and fortune, he had to attend to his duties. He went as an ordinary engineer to Angouleme, but he did not forget his illuminating gas, and he strongly regretted Paris, which he termed "an incomparable focus of study." He devoted himself to mathematics and science, he made himself beloved by all, and his mind wandered far from his daily occupation. The engineer in chief soon complained of him, but a committee appointed to investigate the charges that had been made against him affirmed that he was free from any reproach. He was sent back to his post, but war was decimating the resources of France, and the republic, while Bonaparte was in Italy, no longer had any time to pay its engineers. Lebon wrote some pressing letters to the minister, asking for the sums due on his work, but all of them remained without reply. His wife went to Paris, but her applications were fruitless. She wrote herself to the minister the following letter, which exists in the archives of the School of Bridges and Roads: