As for the English soft-paste porcelain of the eighteenth century, there is a remarkable dearth of information both as to its composition and as to its manufacture. We know in fact in much greater detail how the great potteries at King-te-chen were carried on at the same period, thanks to the letters of the Père D’Entrecolles, and to the information collected in Dr. Bushell’s great work, Oriental Ceramic Art (New York, 1899. I shall always quote from the text edition).
The following technical notes are based chiefly on the processes in use either at Sèvres or in the great factories of the Limoges district.[7] To begin with the Kaolin, the ‘premier’ element in the composition of porcelain. The greatest care is taken to procure a pure white clay which should approach as near as possible to the more or less theoretical mineral kaolinite, i.e. to a hydrous silicate of alumina. With this object the rough china-clay brought from the pit is thrown into a large tank of water and broken up with wooden spades; the milky liquid is now decanted into a second tank, leaving behind most of the quartz and the other stony particles. On its way the soup-like liquid passes through the meshes of a sieve—these may be formed either of brass wire or sometimes of finely woven silk. On this sieve all but the finest particles are retained. The greater part of the kaolin is deposited in this second tank, but a certain portion still remains suspended in the liquid, which is again decanted; the remaining kaolin then settles down in the third tank, yielding the finest clay. To dry this slimy mass, it is first forced by hydraulic pumps into canvas bags, and these bags are then pressed between fluted wooden trays, strongly clamped together. We have now got a white chalky mass which may contain as much as 98 per cent. of the hydrated silicate of alumina.
The other materials, the china-stone[8] and the quartz, have first to be reduced to the finest powder. To effect this they may, to begin with, be roasted to effect disintegration, then crushed in a stone-breaking machine, and finally passed through the grinding-pan in which they are ground fine between large blocks of chert which rotate upon a pavement of the same stone. The finely ground materials have now to be mixed in suitable proportions either by the old process of ‘slop-blending,’ where the different ‘slops,’ each of known specific gravity, are run in due proportion into the big ‘blending ark,’ or, as is now usual in the case of fine wares, by weighing out the materials in a dry state. On the relative amounts of the three elements, the china-clay, the china-stone, and the quartz, the nature of the porcelain after firing will depend. M. Vogt (La Porcelaine, Paris, 1893) gives a useful table showing the limits within which the materials may be varied. We may note that in the case of a normal china-stone or petuntse being used instead of felspar, very little additional quartz is required. These limits are: kaolin, 35 to 65 per cent.; felspar, 20 to 40 per cent.; and quartz, 15 to 25 per cent. The larger the percentage of the first material, the harder and more refractory will be the resultant porcelain.
This question of the composition of the paste has been the subject of many experiments lately at Sèvres. A somewhat animated discussion has raged around it. M. Vogt, who is the director of the technical department in the National Porcelain Works, is well qualified to speak on the subject. We shall not hesitate then to avail ourselves of the conclusions which he arrives at, the more so as they put tersely some important points of which we shall see the importance later on. I refer especially to the relations of the glazes and the coloured decorations to the subjacent paste.
These are, then, the results that M. Vogt arrives at:—
The two extreme types of porcelain, one with 65 per cent. of kaolin and the other with only 35 per cent., when taken from the kiln do not differ in appearance, though one has been subject to a temperature of 1500° C. to ensure vitrification and the other to only 1350° C. Their physical properties, however, are very different. The first, rich in alumina derived from the excess of kaolin, stands without injury variations of temperature, it suits well with a glaze made from felspar, a glaze hard enough to resist the point of a knife. These are excellent qualities for domestic use, but such porcelain does not lend itself well to artistic decoration. At the high temperature required in this case in the firing, the colours of the paste and of the glazes assume dull and tame hues, so as to offer little resource to the artist. In a word, in that part of the decoration that has to be subjected to the full heat of the kiln, the artist has command only of a restricted and relatively dull palette. Again, in the decoration of the muffle-stove the vitrifiable enamels do not become incorporated with the glaze on which they rest. If a decoration in opaque or translucent enamels is attempted, these enamels are apt to split off, carrying with them a part of the glaze. To sum up: the porcelain of which the hard paste of Sèvres, introduced by Brogniart, may be regarded as a type, though excellent for domestic use, is incapable of receiving a brilliant decoration.
Porcelain of the second type, more silicious and less aluminous, is fired at a lower temperature. In order to get a glaze sufficiently fusible to melt at such a temperature to a fine uniform surface, it is necessary to introduce a certain amount of lime into its composition; by this the glaze is rendered at the same time a little softer. But now the lower temperature of the fire will allow of a greater variety and greater brilliancy in the colours either combined with or used under the glaze. When we come to the muffle-fire we can employ enamels of the widest range of colour, yielding a brilliant decoration. On the other hand, this type of porcelain offers less resistance than the other to the action of hard bodies and to rapid changes of temperature—enough resistance, however, so M. Vogt thinks, for all ordinary usages. It is to this type that the porcelain of China, and Japan, as well as the ‘new porcelain’ of Sèvres belongs. The latter comes nearer to the porcelain of the East than any other European ware. Finally, M. Vogt points out that most of the other European porcelains, those made in the Limoges district, in Germany and in Denmark, are of an intermediate type, and that they allow the use of either a felspathic or of a calcareous glaze (Vogt, La Porcelaine, pp. 144 seq.).[9]
To return to our raw materials, which we may now suppose to be weighed out in a dry state in the required proportions. These are once more thoroughly mixed with water to form the slip or barbotine, which is again passed through a fine sieve. To remove any particles of iron which may have come from the machinery or elsewhere, and which if allowed to remain would form unsightly stains on the finished ware, it is usual to pass the slip at this stage through a vessel in which a number of horse-shoe magnets are suspended. In some of the large French factories a more complicated machine is used for this purpose. The superfluous water has now to be removed either by evaporation or by pressure between canvas bags in the manner described above. The paste may then be passed through a pug-mill to render it uniform in consistency.
A curious question arises with regard to the prepared clay. There was formerly a widespread idea, which may contain an element of truth, that instead of handing the clay at once to the potter, it should be kept, under certain conditions, for a long space of time that it may undergo a process of ‘aging’ and fermentation. By the ‘aging,’ the working qualities, especially of a ‘short’ or non-plastic paste (such as that in use at Sèvres in the eighteenth century, in making the pâte tendre), were doubtless increased, the more so when the clay was at intervals subjected to fresh kneading and watering. With regard to the long periods for which the clay was kept by the Chinese, the most exaggerated statements were formerly made. Mr. William Burton is of opinion that there may be in some cases an evolution of carbonic acid and sulphuretted hydrogen when natural plastic clays are used, for these may contain both vegetable remains and small quantities of iron pyrites. But the change, he thinks, is chiefly a physical one, due to the settling down of the mass. Might there not also, I would suggest, be a change of a more intimate nature, due to the formation of gelatinous silica and perhaps also of fresh alkaline or other silicates, among these minutely comminuted particles of various materials now freshly brought together? We know very little of the conditions that give to natural clays their peculiar unctuous quality and their plasticity.
We come now to what has been called the ‘shaping’ of the clay, using that word as an equivalent to the French façonnage to include all the processes, throwing on the wheel, turning of the lathe, ‘pressing’ and ‘casting,’ by which the desired form is given to the vessel.