Gelation Temperature of a Gelatin Solution 

Prepared by Frédéric Mondiot at LS Instruments AG

March 2014

 

Image contains a link to PDF "Gelation Temperature of a Gelatin Solution"

Download PDF

 
 

Introduction

Diffusing Wave Spectroscopy (DWS) is a modern light scattering technique that is mainly utilized to probe the motion of particles in colloidal media.[1] A microrheological analysis of the particle motion may further provide the medium’s rheological properties, namely the frequency-dependent storage and loss moduli, G’(ω) and G’’(ω), respectively.[2] DWS can be applied to a rich variety of soft-matter systems, including gelling systems. In particular, DWS is able to accurately characterize their gel point, defined when the normalized intensity correlation function (ICF) no longer decays to zero.[3] Gelatin solutions (Figure 1a) are dispersions of biopolymers in water that form physical gels below the gelation temperature Tgel (Figure 1b).[4,5] Furthermore, at the gelation temperature of polymeric gel-forming liquids, G’ ~ G’’ ~ ωn, where 0.19 < < 0.92.[6] In this application note, we propose to determine Tgel of a food grade gelatin solution using the DWS RheoLab from LS Instruments.

 

 a) liquid above gel point and b) gel phase below gel point of the gelatin solutions containing 1 wt% of 784 nm diameter polystyrene particles.

Figure 1. a) liquid and b) gel phases of the gelatin solutions containing 1 wt% of 784 nm diameter polystyrene particles.

 
 

Sample Preparation

 

Commercial gelatin was dissolved at 2.5 wt% (weight by weight) in deionized water at T = 50°C. To perform DWS on this transparent mixture, 784 nm diameter tracer polystyrene particles (microParticles GmbH®) were added at a concentration of 1 wt%. At such a particle concentration, the sample appears white (Figure 1). Subsequently, the solution was introduced into a 5 mm thick glass cuvette at 50°C, which was loaded in the DWS RheoLab. Then, the gelatin solution was progressively cooled from 50°C to 15°C, with temperature steps of 5°C down to 30°C, and steps of 0.5°C from 30°C. At each temperature, a waiting time of 30 min was observed before measuring. Cooling rate was shown not to influence the gel point of gelatin.[7,8] The transport mean free path l* of the sample was determined using the DWS RheoLab;l* was 290 μm over the temperature range studied.

 
 

Results and Discussion

 

In the liquid phase above Tgel,the ICFs, obtained in transmission, decay to zero, but remain finite in the gel phase below Tgel (Figure 2a). As the sample is further cooled in the gel phase, however, the height H of the plateau of the ICF curves at large values of τ is observed to increase (Figure 2). To quantify the latter observation, the normalized ICFs were fitted using the following function: f(τ) = A x exp(-τ/τC) + H, where A and τC are the amplitude and the characteristic time of the decay, respectively. According to Schurtenberger et al.,[3] the definition of the gel point is when H rises from zero. Therefore, Tgel = 22.5°C.

 

a) ICFs measured when cooling the sample (an arrow indicates the direction of the curve change), b) H and G’(ω=100 rad.s-1) vs. T.

Figure 2. a) ICFs measured when cooling the sample (an arrow indicates the direction of the curve change), b) H and G’(ω=100 rad.s-1) vs. T.

 

In addition, the increase of H with further decrease of T to 15°C is a consequence of the progressively restricted particle motion. This is due to the strengthening of the forming gel, as shown in Figure 2b, where H follows the same trend as the elastic modulus G’, taken at ω = 100 rad.s-1. After automatically extracting the particle mean square displacement (MSD) from the ICFs (Figure 3a), the DWS RheoLab software can accurately compute both G’(ω) and G’’(ω) upon application of the Generalized Stokes-Einstein Relation (GSER) to the particle MSD (Figure 3b).[2] In the liquid phase, the MSD and G’’ are linear with τ and ω respectively, indicating a purely viscous fluid. In the gel phase, the MSD and G’ saturate at long τ and low ω values respectively. This reflects the elastic behavior of the medium. At Tgel as defined above, MSD ~ τ0.8, andthe relation G’ G’’ ωn with n = 0.8 is verified. Moreover, the magnitude of n is consistent with values previously obtained for similar systems.[4-5]

 

a) MSDs, b) Microrheology curves computed by the DWS RheoLab software from the MSDs using the GSER.

Figure 3. a) MSDs, b) Microrheology curves computed by the DWS RheoLab software from the MSDs using the GSER.

 
 

Conclusion

 

Using the DWS RheoLab, we have successfully and unambiguously determined the gelation temperature Tgel of a commercial, food grade gelatin solution as Tgel = 22.5°C. Aging of gelatin gels could be further studied using the DWS RheoLab since it facilitates time‑dependent measurements.

 

References

 

[1]   D.A. Weitz, D.J. Pine, Diffusing-Wave Spectroscopy. In Dynamic Light Scattering; Brown, W., Ed.; Oxford

       University Press: New York, 1993, 652-720.

[2]   T.G.Mason, D.A.Weitz, , Optical Measurements of Frequency-Dependent Linear Viscoelastic Moduli of Complex Fluids,

       Phys. Rev. Lett., 1995, 74, 1250-1253.

[3]   S. Romer, F. Scheffold, P. Schurtenberger, Sol-Gel Transition of Concentrated Colloidal Suspensions, Phys. Rev.

       Lett., 2000,85, 4980-4983.

[4]   J. Peyrelasse, M. Lamarque, J.P. Habas,  N. El Bounia, Rheology of Gelatin Solutions at the Sol-Gel Transition,

       Phys. Rev. E, 1996, 53, 6126-6133.

[5]   T. Matsunaga, M. Shibayama, Gel Point determination of Gelatin Hydrogels by Dynamic Light Scattering and

       Rheological Measurements,  Phys. Rev. E, 2007, 76, 030401 (R).

[6]   R.G. Larson, The Structure and Rheology of Complex Fluids. Gubbins K.E., Ed.; Oxford University Press: New York,

       1999, 232-260.

[7]   H.B. Bohidar, S.S. Jena, Kinetics of sol-gel transition in thermoreversible gelation of gelatin, J. Chem. Phys., 1993,

       98, 8970-8977.

[8]   The gel point of other colloidal systems could be cooling-rate dependent.