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Intensity and linewidth measurements of light scattered by the isobutyric acid in water system are reported for various equilibrium states in the critical neighborhood of the temperature-concentration diagram. By extrapolation of these data to zero scattering angle and then to (unrealized) states below the phase separation temperature one may determine a common "pseudospinodal curve" Tₛₚ(X) described by Tc-Tₛₚ(X)~|X-Xc|^1β^ where X is the concentration, and we find β^0.37±0.04. As expected on the grounds of the homogeneity hypotheses, the value of β^ is essentially the same as the previously observed value of the exponent β for the coexistence curve. Empirical equations of the form IC,0^_^-1∝[T-Tₛₚ(X)]^γ and D∝[T-Tₛₚ(X)]^γ* are used to effect the extrapolations to determine Tₛₚ(X). Here IC,0 and D are the extrapolated zero-angle scattering intensity and the diffusion coefficient, while γ and γ* are corresponding critical exponents. We show theoretically, however, that a value β^≠1/2 is inconsistent with the general validity of these empirical formulas, which should thus be discarded as over-all representations of the variations of D and IC,0. A tentative test is made of a more general scaling equation for IC,0 by a convenient plot. Moderate success is obtained. The measurements confirm the exponent values γ=1.24±0.03 and γ*=0.67±0.03. The distinction between pseudospinodal curves, determined by extrapolation from stable thermodynamics states, and a true spinodal curve which (if it exists) can only be observed by measurements on metastable states, is emphasized.
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Chu et al. (1969) studied this question.
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