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Photon Correlation Spectroscopy Study of Diffusion of Gelatin Chains and Surfactant Complexes


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1 School of Physical Sciences, Jawaharlal Nehru University, New Delhi-110 067, India
     

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Photon Correlation Spectroscopy (PCS) study carried out on semi-dilute, 4%(w/v) aqueous gelatin sols with the anionic surfactant, sodium dodecyl sulphate (SDS) showed three relaxation processes in the dynamic structure factor data; first an exponential process S (q,t) ~ exp (-Df(q2t) at t ≤ 20 μs called the gel mode, was observed followed by an intermediate power law regime S(q,t) ~ t(q) at 20 μS ≤ t ≤ 1 ms and finally a stretched exponential decay S(q,t) ~ exp -(t/τc)β observed for t ≥ 1 ms. The power-law exponent (α) and characteristic time τc in stretched part were found to be q-dependent, α ~ qX with x = 1.80 ± 0.09 in the sol state; and τc~q-y, y = 2.05 ± 0.08 also in the sol state but independent of SDS concentration. The temperature dependence of α and τc was measured. With SDS the different characteristic length scales alter the conformation of gelatin. Our results agree with the predictions of anomalous Gaussian diffusion model in the sol state.

Keywords

Photon Correlation Spectroscopy, Relaxation, Sol-Gel Transition, Diffusion.
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  • Photon Correlation Spectroscopy Study of Diffusion of Gelatin Chains and Surfactant Complexes

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Authors

Saroj Maity
School of Physical Sciences, Jawaharlal Nehru University, New Delhi-110 067, India
H. B. Bohidar
School of Physical Sciences, Jawaharlal Nehru University, New Delhi-110 067, India

Abstract


Photon Correlation Spectroscopy (PCS) study carried out on semi-dilute, 4%(w/v) aqueous gelatin sols with the anionic surfactant, sodium dodecyl sulphate (SDS) showed three relaxation processes in the dynamic structure factor data; first an exponential process S (q,t) ~ exp (-Df(q2t) at t ≤ 20 μs called the gel mode, was observed followed by an intermediate power law regime S(q,t) ~ t(q) at 20 μS ≤ t ≤ 1 ms and finally a stretched exponential decay S(q,t) ~ exp -(t/τc)β observed for t ≥ 1 ms. The power-law exponent (α) and characteristic time τc in stretched part were found to be q-dependent, α ~ qX with x = 1.80 ± 0.09 in the sol state; and τc~q-y, y = 2.05 ± 0.08 also in the sol state but independent of SDS concentration. The temperature dependence of α and τc was measured. With SDS the different characteristic length scales alter the conformation of gelatin. Our results agree with the predictions of anomalous Gaussian diffusion model in the sol state.

Keywords


Photon Correlation Spectroscopy, Relaxation, Sol-Gel Transition, Diffusion.