THE MEASUREMENT of pH provides a relative estimation of the deterioration of cotton resulting from field weathering under humid conditions that may prevail between opening of the bolls and picking. These are the same conditions that contribute to the development of a high free fatty acid content in cottonseed before picking. Weathered cotton exhibits a decrease in organic acid content and an increase in pH [7,8] . These changes are brought about by the use of organic' acids as nutrients by microorganisms, leaving the potassium of the salts of the organic acids in the fiber as the carbonate. Rain may leach some of the organic and inorganic salts, with the result that the alkalinity determined on the ash of a unit quantity of the cotton may be reduced [8]. In addition, it has been demonstrated that the growth of microorganisms may alter the physical properties of the fiber, particularly the breaking strength and surface properties [2, 3].Current methods for determining pH in cotton fiber employ an aqueous extraction of the fiber, followed by either an electrometric or colorimetric determination of the pH of the extract. Representative procedures are described by McCall et al. [8], Marsh et al. [7], and Hall and Elting [3]. Wakeham and Skau [9] demonstrated that the pH of an aqueous extract of cotton fabric is a function of the amount of water used for the extraction. These authors determined the pH of successive dilutions of an aqueous extract of the fabric, followed by extrapolation to zero dilution in order to define the pH in terms of the amount of water present in the fabric equilibrated to the standard atmosphere of 65% R.H. and 75 ° F. Although precise, this method does not satisfy the requirements for routine use where speed and simplicity are essential. The purpose of this paper is to present a colorimetric method by which indicator solutions are applied directly to the fiber. This approach should minimize the dilution effect and thereby achieve a close estimation of the actual pH of the fiber. * One of the laboratories of the Bureau of Agricultural and Industrial Chemistry, Agricultural Research Administration, U. S. Department of Agriculture.
Basis of the MethodSulfonphthalein indicators were chosen since they offer an easily distinguishable gradation of color with changing pH, and since neutralization of the sulfonic acid groups permits their use in poorly buffered systems [6]. Aqueous solutions of indicators were not employed due to the difficulty of wetting raw cotton. Early attempts to use neutralized sulfonphthalein indicators in essentially nonaqueous solutions of acetone and alcohols were unsuccessful, probably due to the insolubility of the noncellulosic constituents of the fiber in the organic solvents. It was found that solutions of these indicators in aqueous alcohols were more satisfactory; however, with the higher concentrations of alcohol the color change was less sensitive. A solution of the indicator in aqueous isopropyl alcohol (25% alcohol by volume) proved most satisfactory. This concen...