A Text-book of Tanning: A treatise on the conversion of skins into leather, both practical and theoretical.Procter, H. R. (Henry Richardson)
Science
A Text-book of Tanning: A treatise on the conversion of skins into leather, both practical and theoretical.
Procter, H. R. (Henry Richardson)
Tanning
Having described the products of decomposition, something must be
said of the way in which these constituents are combined to form the
unaltered tannins. The only tannin of which we have as yet anything
approaching complete knowledge is that obtained from galls, sumach, and
myrabolans, and which is thence called gallotannic acid.
_Gallotannic, or digallic acid_ exists as the principal tannic acid
of the galls of oak, tamarisk, &c.; and, in mixture with more or less
ellagitannic acid, in myrabolans, divi-divi, sumach, pomegranate rind,
and many other plant-products. It has also been formed by Schiff from
gallic acid, by mixing it, after drying at 230° F. (110° C.), with
phosphorus oxychloride to a thin paste, and heating, first to 212° F.
(100° C.) and then to 248° F. (120° C ). Much hydrochloric acid was
evolved, and the gallic acid was converted into a yellow powder, which
after purification by washing with ether, dissolving in water, allowing
the gallic acid to crystallise out, saturating with salt, washing the
precipitated tannin in salt solution, and redissolving in alcohol and
ether, had all the reactions of purified gall tannin, but was perfectly
reconverted into gallic acid on boiling with hydrochloric acid, without
the formation of any trace of ellagic acid, or glucose. By analysis of
the tannin and its acetyl compounds it was shown to be digallic acid,
and its constitutional formula is almost certainly as follows:--
{CO.OH
{OH
C_{6}H_{2}{
{OH
{O }
}
{CO}
{OH
C_{6}H_{2}{OH
{OH
By boiling gallic acid with solution of arsenic acid, Schiff obtained a
product which precipitated gelatin, and otherwise reacted like tannin,
and he regards this as digallic acid, but other experimenters have
failed to obtain digallic acid by this means, and have found that on
complete removal of arsenic, the compound was reconverted to gallic
acid. It therefore remains a moot point whether digallic acid is really
formed, and reconverted into gallic acid by the prolonged action of
hydric sulphide, which is necessary to remove the arsenic, or whether,
as seems more probable, the supposed tannin is merely an arsenical
compound of gallic acid.
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