Large deformation and instability in gels Zhigang Suo Harvard University 1 Gel = elastomer + solvent Elasticity: long polymers are cross-linked by strong bonds. Fluidity: polymers and solvent molecules aggregate by weak bonds. reversible Thermodynamics of swelling •Entropy of mixing •Entropy of contraction •Enthalpy of mixing 2 Ono, Sugimoto, Shinkai, Sada, Nature Materials 6, 429, 2007 Gels in daily life Jelly Contact lenses Wichterie, Lim, Nature 185, 117 (1960) Drug delivery Ulijn et al. Materials Today 10, 40 (2007) Tissues, natural or engineered 3 Gels in engineering Ion exchange for water treatment Sealing in oil wells Shell, 2003 Valves in fluidics Beebe, Moore, Bauer, Yu, Liu, Devadoss, Jo, Nature 404, 588 (2000) 4 THB theory ui - solid displacement εij 21 ui , j u j ,i - strain Stress-strain relation σ ij 2Gεij vi 0 neglect liquid motion Equilibrium equation σ ij , j f ui 0 t body force due to friction 2Gνεkk δij 1 2ν Limitations No instant response to loads Linear theory, small deformation Basic principles are unclear, hard to extend 5 Tanaka, Hocker, and Benedek, J. Chem. Phys. 59, 5151 (1973) Multiphasic theory biphasic theory List of Equations A nonionic polymeric gel is a mixture of two phases: network (n) and solvent (s). Mass conservation ρn ρn v n 0 t s ρ ρs v s 0 t Balance of linear momentum Dn v n σ n ρ n bn π n Dt Ds v s ρs σ s ρ s bs π s Dt where the material derivative with respect to phase α ρn Helmholtz free energy for each species α D vα , D t and π α is the momentum supply to α component from the other phase n A T ,C , ρ , ρ A n e n Ts n A n T ,C, ρ n , ρ s s π π 0 A s e s Ts s Energy conservation Dn e n σ n : v n q n ρnr n ε n Dt Dses ρs σ s : v s q s ρsr s ε s Dt Second law of thermodynamics ρn Dn s n qn rn Ds s s qs rs ρn ρs ρs 0 Dt T T Dt T T α where s is the entropy density of α component, and the Helmholtz free energy density A n e n Ts n A n T ,C , ρ n , ρ s s n s ρn Incompressibility A s e s Ts s A s T ,C , ρ n , ρ s φ v φ v v v φ 0 n n s s s n View solvent and solute as two phases s where the volume fraction φ α is related to the density as ρα φα ρ0α . The constitutive relations: An A s T σ n φn λI 2F ρn ρs F C C An A s σ s φ s λI ρ s ρn ρs I s ρ ρ s π n π s λφn ρn An ρ s ρ s ρ sC : Is the theory applicable to gels? A s f vs vn C Unclear physical picture. Unmeasurable quantities. Bowen, Int. J. Eng. Sci. (1980) Lai, Hou, Mow, J. Biomech. Eng. Trans. (1991) 6 Our preference: monophasic theory • Regard a gel as a single phase. • Start with thermodynamics. Gibbs, The Scientific Papers of J. Willard Gibbs, pp. 184, 201, 215 (1878): Derive equilibrium theory from thermodynamics. (This part of his work seems less known.) Biot, JAP 12, 155 (1941): Use Darcy’s law to model migration. Poroelasticity. …… Hong, Zhao, Zhou, Suo, JMPS (2007). http://dx.doi.org/10.1016/j.jmps.2007.11.010 7 System = gel + weight + solvent M work done by the pump Pump, Pl work done by the weight Solvent F l , M Helmholtz free energy of gel M Equilibrium condition p p0 v kT log p / p0 Gel = Network + M solvent molecules F Pl M P F l , M l F l , M M l Weight, P 8 Field variables Equilibrium condition F Pl M l L C M AL s P A Reference state Current state M=0 W s C s W λ , C λ μ A pump Pump, M gel P l M AL AL l AL L F M W λ , C C W , C Helmholtz free energy per volume l P weight 9 3D inhomogeneous field Deformation gradient FiK Concentration Free-energy function xi X, t X K C X, t W F, C Equilibrium condition WdV B x dV T x dA CdV i i i i pump Equivalent equilibrium condition siK W F, C FiK siK Bi 0 X K Gibbs (1878) W F, C C Gel Weight siK N K Ti 10 Flory-Rehner free energy Swelling increases entropy by mixing solvent and polymers, but decreases entropy by straightening the polymers. Free-energy function Free energy of stretching Free energy of mixing W F, C Ws F Wm C Ws F 21 NkTFiK FiK 3 2 logdet F Wm C kT v 1 χ vC log 1 vC 1 vC 11 Flory, Rehner, J. Chem. Phys., 11, 521 (1943) Molecular incompressibility + = Vdry + Vsol = Vgel 1 vC det F v – volume per solvent molecule Assumptions: – Individual solvent molecule and polymer are incompressible. – Gel has no voids. (a gel is different from a sponge.) 12 Equations of state Enforce molecular incompressibility as a constraint by introducing a Lagrange multiplier siK W F, C H iK detF FiK W F, C v C Use the Flory-Rehner free energy siK NkT FiK H iK H iK det F NkT vC 1 kT log v 2 1 vC 1 vC 1 vC s1 NkT 1 11 23 s2 1 2 2 3 1 s3 NkT 3 31 12 13 Inhomogeneous equilibrium state Core Empty space R A0 r A B Dry polymer Gel (a) Reference State b (b) Equilibrium State Concentration is inhomogeneous even in equilibrium. Stress is high near the interface (debonding, cavitation, wrinkles). 14 Zhao, Hong, Suo, APL 92, 051904 (2008 ) Hydrogel-actuated nanostructure = 1.5 0 -0.3 = 0.1 Nv = 10-3 RH = 80% vG/kT -0.4 -0.5 -0.6 -0.7 RH = 95% -0.8 RH = 100% -0.9 -1 -0.5 Experiment: Sidorenko, Krupenin, Taylor, Fratzl, Aizenberg, Science 315, 487 (2007). Theory: Hong, Zhao, Suo, http://imechanica.org/node/2487 0 (rad) 0.5 1 15 Critical humidity can be tuned 1.4 1.2 = 1.7 (rad) 1 0 0.8 0.6 1.2 0.4 0.2 0 0 1.1 = 0.1 Nv = 10-3 20 40 60 Relative humidity (%) 80 100 16 Hong, Zhao, Suo, http://imechanica.org/node/2487 Crease Tanaka et al, Nature 325, 796 (1987) Denian 17 L (a) A' Our model L O A reference state U U L2 f (b) A' O A ε ε homogeneous state U L2 f (c) A/A' ε O c ε creased state Linear perturbation, Biot (1963), biot 0.46 Experiment, Gent, Cho, Rubber Chemistry and Technology 72, 253 (1999) Our model 18 c 0.35 Elasticity with huge volumetric change Equilibrium condition Legendre transform WdV B x dV T x dA CdV i i i i W C dV B x dV T x dA i An alternative free-energy function Recall i i i ˆ W C W W siK FiK C ˆ s F C W iK iK ˆ F, W siK FiK ABAQUS UMAT ˆ F, W C Liu, Hong, Suo, manuscript in preparation. 19 Time-dependent process Shape change: short-range motion of solvent molecules, fast Volume change: long-range motion of solvent molecules, slow 20 Hong, Zhao, Zhou, Suo, JMPS (2007). http://dx.doi.org/10.1016/j.jmps.2007.11.010 Coupled deformation and migration pump Deformation of network Conservation of solvent molecules xi X, t FiK X K C X, t J K X, t r X, t t X K t JK NK Gel i X, t t Weight Nonequilibrium thermodynamics WdV B x dV T x dA rdV idA i Local equilibrium W F, C siK FiK W F, C C Biot, JAP 12, 155 (1941) i i i Mechanical equilibrium siK X, t Bi 0 X K siK N K Ti Rate process J K M KL X, t X L 21 Hong, Zhao, Zhou, Suo, JMPS (2007). http://dx.doi.org/10.1016/j.jmps.2007.11.010 Ideal kinetic model Solvent molecules migrate in a gel by self-diffusion J K M KL X L Diffusion in true quantities ji cD μ kT x i Conversion between true and nominal quantities ji FiK X K xi FiK JK det F M KL D H iK H iL det F 1 vkT 22 Hong, Zhao, Zhou, Suo, JMPS (2007). http://dx.doi.org/10.1016/j.jmps.2007.11.010 Diffusion of labeled water Stokes-Einstein formula Dself kT / 6R 8 1010 m 2 /s polymer volume fraction Muhr and Blanshard, Polymer, 1982 23 Diffusion or convection? ~50 Ds D = 410-8 m2/s Tokita, Tanaka, J. Chem. Phys, 1991 • • Macroscopic pores? Convection? 24 Swelling of a thin layer solvent relative swelling gel dimensionless time Fitting swelling experiment is hard: Missing data Fick’s law: Concentration is not the only driving force TBH theory also has problems 25 Zhou, Zhao, Hong, Suo, unpublished work (2007) Summary • Gels have many uses (soft robots, drug delivery, tissue engineering, water treatment, sealing in oil wells). • Mechanics is interesting and challenging (large deformation, mass transport, thermodynamic forces, instabilities). • The field is wide open. 26