Abstract The want of a chemical method to determine incipient decomposition in preserved latex has been long felt by producers and consumers of latex. A method often used is to neutralize the ammonia in latex with boric acid or sulfuric acid, and to judge the extent of decomposition from the intensity of putrefactive odors. This method, besides having limitations common to all subjective tests, is insufficiently sensitive to detect the early stages of putrefaction. Another way of assessing deterioration in latex is to determine the total concentration of acidic substances by KOH titration. Though it is widely used in industry, the method has several disadvantages, both as a test for decomposition and as an index of processing behavior. First, acids are estimated which titrate up to pH 11.2, thus failing to discriminate between stabilizing (i.e. soap forming) and destabilizing (e.g. formic, acetic) acids. Second, conjugate acids of bases, basic groups of zwitterions from amino acids, etc., are included. Third, it fails with latexes to which soaps or fixed alkalies have been added. Following observations made in 1941 by the late W. S. Davey at the Rubber Research Institute of Malaya, we have now shown that a substantial proportion of the acids formed in latex as a result of natural degradation processes can be distilled in steam, and that these volatile acids consist mainly of acetic acid, with some formic and propionic acids. It is considered that a test of spoilage based on the estimation of these acids would be free from the disadvantages that are inherent in the KOH titration, and methods of determining quantitatively the volatile fatty acids in latex have accordingly been worked out.
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