The heat evolved by the decomposition of the acetylene by the formation of the hydrochloric acid in the last equation is then propagated amongst the rest of the gaseous mixture, accelerating the action, and causing the acetylene to react with the chlorine to form more hydrochloric acid and free carbon thus; C_2H_2 + Cl_2 = 2HCl + C_2. It is evident that these results do not altogether explain the mechanism of the reactions involved. Possibly the formation of substitution products and the consequent occurrence of an explosion is brought about by some foreign substance which acts as a catalytic agent. Such substance may conceivably be one of the impurities in crude acetylene, or the solid matter of a bleaching-powder purifying material. The experiments at least indicate the direction in which safety may be sought when bleaching- powder is employed to purify the crude gas, viz., dilution of the powder with an inert material, absence of air from the gas, and avoidance of bright sunlight in the place where a spent purifier is being emptied. Unfortunately Nieuwland did not investigate the action on acetylene of hypochlorites, which are presumably the active ingredients in bleaching- powder. As will appear in due course, processes have been devised and patented to eliminate all danger from the reaction between acetylene and chlorine for the purpose of making tetrachlorethane in quantity. Acetylene combines with hydrogen in the presence of platinum black, and ethylene and then ethane result. It was hoped at one time that this reaction would lead to the manufacture of alcohol from acetylene being achieved on a commercial basis; but it was found that it did not proceed with sufficient smoothness for the process to succeed, and a number of higher or condensation products were formed at the same time. It has been shown by Erdmann that the cost of production of alcohol from acetylene through this reaction must prove prohibitive, and he has indicated another reaction which he considered more promising. This is the conversion of acetylene by means of dilute sulphuric acid (3 volumes of concentrated acid to 7 volumes of water), preferably in the presence of mercuric oxide, to acetaldehyde. The yield, however, was not satisfactory, and the process does not appear to have passed beyond the laboratory stage.