Pyroligneous acid

Definition and stakes

Josef Bersch,  The manufacture of mineral and lake pigments (1901)

“ Strong pyroligneous acid may be used, its empyreumatic odour is without influence on the quality of the product. The pan is heated until the contents almost, but not quite, boil. They are frequently stirred so that the particles at the bottom are brought in contact with the acid. A dark green solution is formed; when its colour no longer increases in depth it is allowed to stand until suspended solids sink to the bottom. The clear solution is then drawn off and rapidly evaporated in shallow copper pans. It is important that the liquid should not contain an appreciable quantity of free acid. ”
Source: Gutenberg

Various,  Notes and Queries, Number 216, December 17…

“ Should the picture be very tardy, either from an insufficient exposure, want of light, or other cause, a few drops of a solution of pyrogallic acid, made with 3 grains to the ounce of water, and a drachm of acetic acid, will act very beneficially. It sometimes gives an unpleasant redness upon the surface, but produces great intensity upon looking through it. Until the pyrogallic solution was added, there was scarcely anything visible upon the specimen exhibited, the failure having in the first instance happened from the badness of the iodized paper. ”
Source: Gutenberg

1911 Encyclopædia Britannica, Volume 22… (1911)

“ It reduces ammoniacal silver solutions. When heated with hydrochloric acid to 100° C. it yields carbon dioxide and pyrotartaric acid, C5H8O4, and when warmed with dilute sulphuric acid to 150° C. it gives carbon dioxide and acetaldehyde. Sodium amalgam or zinc and hydrochloric acid reduce it to lactic acid, whilst hydriodic acid gives propionic acid. It readily condenses with aromatic hydrocarbons in the presence of sulphuric acid. It is somewhat readily oxidized; nitric acid gives carbonic and oxalic acids, and chromic acid, carbonic and acetic acids. ”
Source: Wikisource

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