Abstract

The elastic modulus and hydrophilicity of cross-linked poly(dimethylsiloxane) (PDMS) are tunable via cross-linker concentration and the addition of a simple surfactant, C12E4, before curing. However, the surfactant concentration, [C12E4], reduces the elastic modulus (73% lower for 6.3% w/w) because it reduces the extent of curing. This is likely because the hygroscopic surfactant results in water poisoning of the catalyst. Three distinct time-dependent hydrophilicity profiles were identified using water contact angle analysis with [C12E4] determining which profile was observed. This indicates the concentration-dependent phase behavior of C12E4 within PDMS films. Changes in phase behavior were identified using small-angle neutron scattering (SANS) and a compatibility study. No surface excess or surface segregation of surfactant was observed at the PDMS–air interface. However, a surface excess revealed by neutron reflectivity against a D2O interface indicates that the increase in hydrophilicity results from the migration of C12E4 to the film interface when exposed to water.

Highlights

  • Poly(dimethylsiloxane) (PDMS) is a polymer that has use in microfluidic devices,[1−4] fouling-release coatings,[5−9] and cell cultivation.[10,11] When cross-linked to form a network, its biocompatibility, low bulk modulus, deformability, low roughness, and low surface energy have made the polymer a favorable material for these applications,[12] and by learning to better control some of these properties, the functionality of PDMS in these applications can be improved.PDMS does have limitations

  • Similar observations regarding the trend in the tangent elastic modulus with cross-linker concentration and the different nonlinear rheologies have been reported by Seghir and Arscott when curing Sylgard 184 for 2 h at 100 °C.66

  • Available PDMS can be tuned by adjusting the concentration of durham.ac.uk the cross-linker used when curing and that the nonlinear rheology is different when using more or less than the concentration of cross-linker recommended by the manufacturer

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Summary

■ INTRODUCTION

Poly(dimethylsiloxane) (PDMS) is a polymer that has use in microfluidic devices,[1−4] fouling-release coatings,[5−9] and cell cultivation.[10,11] When cross-linked to form a network, its biocompatibility, low bulk modulus, deformability, low roughness, and low surface energy have made the polymer a favorable material for these applications,[12] and by learning to better control some of these properties, the functionality of PDMS in these applications can be improved. D2O could not be obtained without enriched layers of d25− C12E4 near the water interface While this increase in SLD could be due to the penetration of D2O into the PDMS matrix, such a layer was not needed to fit the reflectivity curve from a pure PDMS film against D2O (shown in Figure 10), suggesting arises from the phase separation of components into small domains, capable of scattering light. The low-Q Porod exponent of the fit for the 0.87% w/w d25−C12E4 cured sample was ∼2, whereas the higher concentrations showed m ≃ 3 This change in the small-angle scattering behavior between low and high concentrations shows that the low-Q features are likely not inherent to the PDMS matrix.

■ CONCLUSIONS
■ ACKNOWLEDGMENTS
■ REFERENCES

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