January 25, 1918’. THE COLLIERY GUARDIAN 175 ment of the basic open-hearth process, lower silicon content was the practice, round about 1 per cent., while, as the sulphur could be somewhat eliminated in that process, its maximum limit could be raised beyond what was demanded for hsematite iron in the acid pro- cess. The sulphur content, however, must not be excessive. With iron w’ith 1 per cent, silicon and below, it was more difficult to keep the sulphur regu- larly below OTO per cent., and also to control the fur- nace operations, than when making foundry iron or iron for the acid steel process. There appeared to be a wide field for research in the direction of ascertain- ing the best temperature and rate of gasification for each class of coal used, as the coals from different depths had not the same coking power, no less than coals from different districts. The physical composition of the coke was as impor- tant as the chemical. The most important physical characteristic was the hardness or density, which was a measure of its resistance to abrasion or crumbling. A good hard coke would produce more intense heat than soft, also. The efficiency of heat utilisation in a blast furnace depended upon the concentration of heat, and that was best produced by a hard fuel. Hardness Test. Mr. Hewson then described a hardness test made with pieces of an average sample of coke of from J in. to 1 in. across. These were sifted through a Jin. mesh, and the portion remaining on the sieve was taken and dried at 120 degs. Cent., 281b. being weighed and placed in a drum or rattler, together with a dozen cast iron balls 1J in. in diameter. The drum was given 1,000 revolutions in about an hour, and the coke withdrawn and sifted on a J in. mesh, that remaining on the sieve being then weighed and calcu- lated to a percentage of the original weight. That was given as the hardness number. Thus : remaining on Jin. sieve, 271b. 2 oz. ; passed through, 14 oz. ; total, 28 lb.; equalled 96’9 as the hardness. 28 The chemical composition of the coke resolved itself ultimately into the amount of available carbon which it contained, i.e., the quantity of carbon present in the coke in excess of that necessary to melt the slag formed by the ash and sulphur of the fuel, together with the limestone used to flux them. That also was affected by the physical nature of the coke. Accord- ing to Forsythe,, the ash required double its weight of limestone, and the sulphur 3J times its weight to form slag. The slag required 25 per cent, of its weight of carbon to melt it. That, deducted from the fixed carbon, was called “ available carbon.” Mr. Hewson gave a series of analyses and hardness numbers for 18 beehive cokes, in which the hardness numbers ranged from 97-5 to 93’7; and for 12 by-pro- duct cokes, in which the hardness numbers ranged from 97-5 to 91-7. Cokes below 94 hardness, he stated, caused serious trouble in working, and resulted in the furnaces scaffolding or hanging and getting decidedly cold. Cokes below 85 per cent, available carbon had caused irregularities if burdened at the same rate as others, evidently from shortage of heat producing- carbon. Of a number of samples, the best all-round cokes were: a beehive coke which had an analysis of 8-14 per cent, of ash, 0-81 per cent, of sulphur, 91 per cent, of fixed carbon (of which 86-14 per cent, was “available”), and a hardness number of 95-3; and a by-product coke with an analysis of 7-87 per cent, of ash, 0-80 per cent, of sulphur, 91-66 per cent, of fixed carbon (of which 86-94 per cent, was “ available ”), and a hardness number of 97-5. The analytical and physical data, he said, emphasised the desirability of using one class of coke exclusively upon one furnace if sufficient supplies were available. Where such a procedure was adopted, more uniform results in the working of the furnace and the quality of the iron had been observed. Soft Coke. The bad effect of soft coke was cumulative and pro- portionate to its softness, from its liability to crumble during handling between the ovens and the furnace bell, resulting in a large quantity of breeze and small coke being charged into the furnace, and from the crushing of the coke in the furnace. Both these causes resulted in less available carbon reaching the tuyeres than in the case of harder material. The function and behaviour of sulphur in the fur- * nace had been exhaustively investigated by Wuest and Wolff in 1903, who concluded that, contrary to the generally held opinion, the sulphur in the coke does not reach the level of the tuyeres of the blast furnace without undergoing alteration, a great portion of it being previously volatilised by the ascending gases, and then largely absorbed from the gases by the descend- ing charge, in which condition it arrives in front of the tuyeres. Tip to 800 degs. Cent., the sulphur is principally absorbed by the oxides of iron from the sulphur-laden gases, whereas from 800 degs. Cent, upwards, the position is reversed, and the lime becomes the chief absorbent of the sulphur. DISCUSSION. Dr. J. E, Stead (Middlesbrough) wrote that he had never heard of Forsythe, whom Mr. Hewson quoted as an authority. He did not think that Forsythe was a recognised authority. Bell, a long time ago, had stated all, or nearly all, that Mr. Hewson attributed to Forsythe. He did not know whether Mr. Hewson was aware of the fact, but they had had to use the very densest and hardest retort carbon in order to set up the highest temperature in their little furnace for determining the melting point of firebricks, etc. With cold blast, they got up to a maximum temperature of 1,750 degs. Cent., whereas ordinary coke of the porous variety would not give anything like that temperature ; and charcoal—which was still more porous—gave a still lower result; so that there seemed to be some doubt that the hard porous coke was best for giving the highest hearth temperatures. Dr. G. P. Lishman (Lambton Coke Works) wrote that he had always understood that a coke suitable for a blast furnace was one which, though it might readily break down to the size of a fist, was very hard and difficult to crush beyond that point. It seemed to him, therefore, that the hardness test should be taken on lumps of that size, and not on coke broken down to inch pieces. Forsythe’s first desirable charac- teristic was obviously incompatible with a given test made in either way. Mr. G. Weyman (chief chemist of the Newcastle and Gateshead Gas Company) said it was quite an acci- dent to get from the same colliery anything like the same type of coal twice in succession. Most collieries worked several seams of coal, and one never knew what seam one was going to get. Sometimes a trainload itself might be a mixture of two or more seams. An experiment which was carried out recently, in which samples of each truckload of a train of 15 trucks were taken, showed that the ash varied from something like 3 per cent, up to 24 per cent. The samples were taken as w’ell as could be, a good many bucketfuls out of each truck were crushed down, and particular care was taken not to exclude the stone, which was part of the coal so far as the fire was concerned. The variations were enormous, although the average of the whole trainload was probably not more than 10 per cent. He could quite imagine that blast furnace people getting coal with that variable amount of ash might be much disgusted. Phosphorus in Coke. Mr. E. F. Knott (manager of the Priestman Collieries’ Coke Ovens) said that, with regard to density of coke, he thought that, if one got a porous coke, it was very often apt to be soft and easily broken down in the furnace. Mr. Hewson did not mention the question of phosphorus in the coke, a rather impor- tant point, as, in that part of the world, there was a premium placed on a low phosphorus content in coke. The coke represented about three-fourths of a coke oven’s total products, and, if one did not make a good saleable product, and could not get rid of it, one would have to shut down very quickly, and lose all other by-products. He thought it was rather satisfactory that Mr. Hewson’s tables showed that the hardest coke was a patent coke. He noticed that the sulphur in the cokes did not in any way follow the ash content. The highest ash was 13, and contained only 0-84 of sulphur, whereas an ash of only 7 contained even less sulphur than that. As to the variation in coal, he knew of one pit in which there was one seam of coal that was not cokable at all, practically, whilst all the other seams were all right. Mr. W. Diamond (manager of the Marley Hill Coke Ovens of Messrs. John Bowes and Partners, and chairman of the Northern Section of the Coke Oven Managers’ Association) observed that a blast furnace manager could not possibly expect to have the same quality of coke from Derbyshire or South Yorkshire as from Durham, for instance. The coke from Derbyshire was very friable, and had been described as “ pretty rotten.” South Yorkshire was somewhat better, but could not be compared with Durham coke. The density, chemical composition, and mechanical proper- ties of Durham coke far surpassed those of the cokes of the other two counties. In the last 12 or 13 years there had been a considerable improvement in the design of patent ovens. The old ovens took anything up to 50 hours for the carbonisation of South Yorkshire coal, whereas the more modern ones did the work in about 35 hours, and produced a harder coke. At the majority of coke oven installations nowadays there were installed washeries, which, in itself, guaranteed that the coke would be of uniform quality. There were very few such places where the ash rose above 10 per cent. Mr. A. Short (manager of Messrs. Cookson’s Lead Works, formerly of the Priestman Coke Ovens) said that, speaking both as a maker and as a user of coke, the point that struck him was the importance Mr. Hewson attached to the hardness test. There was an extremely small variation in the hardness number— from 98 down to 91. In using coke from a bin, there was an astonishing difference in appearance between that coke and the same coke on the bench. The trans- port made an enormous difference in the appearance of the coke, and that fact certainly made him, as a user of coke, more forbearing than he would otherwise be. He would be very much interested to know what should be the limit of hardness of a coke suitable for blast furnace work. As to the testing of coals for coking, he felt sure that a good deal more should be done by coal owners, who contemplated putting up their own ovens, to get an absolutely reliable test of the coal they were going to treat. For many years a German firm—he was speaking of 15 years ago—had a complete battery of small ovens, in which samples of coals were tested for customers who contemplated putting up their own ovens. He thought it would be very advisable to have a coal testing station on a really big scale—it might have to be a joint concern—in this country. A great proportion of the cost would be covered by the coke and by-products obtained from such a station. There might be ovens of different sizes which could be heated to different temperatures. He had no doubt that the early prejudice against patent coke was very largely due to the fact that the coal was either badly coked in a good oven, or in some other way was not right. Mr. Weyman remarked that gas coke was, of course, not as good as coke oven coke for blast furnaces, but, in some cases, it had been used. In one case, it was rejected because the phosphorus content was too high, but the phosphorus was in the coal to start with. Dr. J. H. Paterson (chief chemist to Messrs. Swan. Hunter and Wigham Richardson Limited) referred to Dr. Stead’s statement as to the temperature produced from the combustion of coke. The speaker had had, within the last few years, a good deal to do with high- temperature reactions, and it had been necessary to make investigations of the reasons for the production of high temperatures with various fuels. Various types of blast furnace coke, ordinary gas coke, and retort carbon had been used for that purpose. It was well known that, if one increased the weight of fuel per cubic inch per minute, one could increase the temperature within limits, and it was quite feasible that, if one could increase the surface of the fuel, one might increase the temperature. The burning of coke or any other fuel, when a blast of air was projected on it, took place at the surface, and the rate at which it burned depended partly on the surface exposed to the blast, but very much more on the capacity of the fuel to absorb oxygen at high temperatures, and to produce what was commonly known as surface combustion in a very intense form. He was inclined to say that, if it were possible to determine—as it had been possible with other materials—how far from the actual surface combustion was taking place in the material, one might get a reason for the production of higher temperatures with some types of carbon. Grading Coke. Mr. C. H. Ridsdale (consulting chemist, Middles- brough) spoke as a practical blast furnace man, and as one who had been associated closely with coke ovens and technically responsible for them for 19 or 20 years. During part of the time that he had been responsible for blast furnace practice, and so on, they graded coke that came into the works, calling the best No. 1, and grading the rest by quarters down to No. 3, which they considered to be too bad to use. The Priestman Collieries’ coke, he mentioned incidentally, always graded as No. 1 for mechanical condition. Mr. Hewson’s paper, in a nutshell, was to the effect that “ bad coke makes bad iron.” That w’as true. Any- one who ivanted to be patriotic must produce good coke, for our military success depended upon good iron. As to porosity, he did not think any coke man need be afraid of making his coke too dense and too hard. The densest coke they could produce was quite porous enough for blast furnace purposes. Of course, a soft coke was very soluble in carbon dioxide in the upper part of the furnace. That was one reason why a manager liked a hard coke. If they got a big coke, like beehive coke, it helped to keep the furnace very open, and now, more than ever, the tendency was to get small ores. If they had small ores and small coke, they could not drive their furnaces. He could tell them positively, as a blast furnace man, that, if they had a ton of coke with 2 cwt. of dead small, it would be very much better if it w7ere practicable to sieve out that 2 cwt., and put only the 18 cwt. into the furnaces. They would get better working, and just as much heat. Mr. Hewson made a great point of the large effect on a furnace working with a comparatively small variation in the condition of the coke. They must consider that matter in connection with what happened in a blast furnace. When carbon burned to CO only, it only gave off 2,473 heat units. In ideal furnace working, they got those 2,473 heat units, and then the CO passed up the furnace and took carbon from the ores in the upper part of the furnace and formed CO2; then they got the burning of that CO and C02, and got another 5,607 heat units. That was when they were working on peroxide ores. In practice, nothing but a pure peroxide ore was reduced in the upper part of the furnace as it ought to be. That w’as only getting an efficiency of 2,300 heat units per unit of coke—not a very abnormal state of things for furnaces on basic and a good many other classes of iron. In that furnace the loss of 1,153 heat units, equivalent to J cwt. of coke, was sufficient to cause a drop in quality of pig from open grey mottled to ordinary white—the former a perfectly good iron for steel making, the latter unsuitable. Secondly, that same J cwt. difference in coke equivalent was equal to a reduction in quality of resulting iron equal to 0-8 cwt. in pig, the iron passing into the slag instead of being reduced, and raising the iron content to 2-44 per cent. The same effect could be produced by a variety of causes, such as leakage of water at the tuyeres, drop in temperature of blast, badly-calcined stone reaching tuyeres, etc., and, amongst others, a drop in quality of the coke used, due to more ash, and hence less carbon, equal to 1’15 per cent. As to the reason that apparently small causes had such marked effects on furnace working, particu- larly w’ith furnaces which, like those on basic, had to use a lot of refractory materials, he made, in 1900, some very careful balance-sheets of heat received and consumed by blast furnaces with coke consumptions varying from 21 to 30 cwt. The data so obtained had constantly proved to be reliable in practice. They showed clearly that, however high the coke consump- tion, of the whole coke charged, most of the heat yielded went in doing what might be termed “ dead ivork,” work the effect of which was not apparent (effecting the necessary chemical changes, heating the escaping gases, etc.), and that it was only the small balance over what was necessary for those purposes, namely, a very small excess of heat, which, once the “dead” requirements were satisfied, produced the effects on the grade of the iron. The effects of small variations of heat available were thus accentuated when they occurred in the hearth. Thus, in the case of a furnace using 27 cwt. of coke, the heat produced by 21 cwt. was used up for purposes other than the fusion of slag and pig, and only that from 6 cwt. w’as used in the hearth for that fusion. Looked at in that light, one got a very different impression of the effect of J cwt. of coke or its equivalent, for it equalled 8J per cent, of all used in the hearth. That explained why any drop in quality, either chemical or mechani- cal, abstracting so large a proportion of the heat from the hearth, told so heavily on the product. As to the size of the coke, the breaking from large to small pieces was not so important as the crushing. If they got “ mush ” that crushed dowm to the small stuff that blew’ out into the flues, and they got it in the dust catchers and the flue dust, and then they had trouble. Friability v. Hardness. Dr. J. T. Dunn (Public Analyst for Newcastle) said that, in regard to coke, the question arose as to what was meant by “ hardness.” One read in the text- books that coke was used instead of charcoal because it was harder, and would bear the burden of the furnace better, but the burden of the furnace could hardly be