Skip to main content

Thank you for visiting You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Dilatancy in the flow and fracture of stretched colloidal suspensions


Concentrated particulate suspensions, commonplace in the pharmaceutical, cosmetic and food industries, display intriguing rheology. In particular, the dramatic increase in viscosity with strain rate (shear thickening and jamming), which is often observed at high-volume fractions, is of practical and fundamental importance. Yet, manufacture of these products and their subsequent dispensing often involves flow geometries substantially different from that of simple shear flow experiments. In this study, we show that the elongation and breakage of a filament of a colloidal fluid under tensile loading is closely related to the jamming transition seen in its shear rheology. However, the modified flow geometry reveals important additional effects. Using a model system with nearly hard-core interactions, we provide evidence of surprisingly strong viscoelasticity in such a colloidal fluid under tension. With high-speed photography, we also directly observe dilatancy and granulation effects, which lead to fracture above a critical elongation rate.


When the volume fraction (ϕ) of a colloidal suspension is increased beyond 50%, its low-shear viscosity increases markedly, and beyond a critical shear stress, the system often displays a shear-thickening or jamming transition1,2,3. The details of this behaviour depend on the nature of the interactions between particles; hard-sphere colloid suspensions represent an important limiting case in which the geometry, rather than the energetics, of particle contacts controls the behaviour. Although jamming transitions in such suspensions have been well investigated in simple shear flows, the same phenomena may be equally relevant in other flow geometries4,5,6.

In the physics of dilatancy7, the volume of a collection of particles must increase on shearing to enable flow. This has been suggested as a possible mechanism for jamming in concentrated colloidal suspensions6. Dilation within a fixed volume of suspending liquid involves the formation of force-transmitting 'clusters', whose growth eventually causes particles to encounter the air–liquid interface. This generates large capillary forces at the free surface, which can then balance the normal inter-particle forces and resist further motion. The colloidal particles can thus form spanning clusters in close contact, jamming the sample. This may then fracture into millimetre-scale 'granules'6. Colloidal granules can be jammed indefinitely by their capillary forces, even though the same volume of fluid and particles can equally well exist as a flowable droplet6.

Jamming of colloids is also seen in pipe and channel flows4,5, where free surfaces are not present. In an extensional rheometer, however8,9, a fluid sample initially forms a cylindrical column surrounded by air, bridging two parallel, horizontal plates. As the upper plate is retracted, a filament forms, which narrows and eventually breaks. This elongational flow, in contrast to more conventional shear and pipe geometries, therefore, implies an increase of the interfacial area during flow. Although purely elongational flow can be achieved by exponential plate separation, a constant separation speed (as used here) is closer to fibre-spinning and other industrial processes. In these, a purely tensile loading creates a mixed flow combining elongation and shear.

Recent studies10,11 have demonstrated that extensional rheometry can successfully be performed on colloidal suspensions. Bischoff White et al.10 measured the tensile stresses of a (ϕ 0.355) cornstarch solution. They observed a flowable filament at low extension rates, but beyond this, found a transition to brittle fracture. The interactions in this system are poorly characterized, but are clearly attractive (see Fig. 1 of ref. 10), presumably because of strong Van der Waals forces. Such interactions could greatly influence the flow behaviour, as they do in strongly aggregating colloids at lower densities10. The fundamental physics of colloidal jamming is therefore better addressed in model systems of nearly hard-sphere particles3,4,5,6, which are forced into contact by external stresses without the added complexities of ill-defined interactions.

Here, we present an experimental study of the stretching of concentrated suspensions of nearly hard-sphere (poly(methyl methacrylate))4,5 particles. We observe that on increasing the applied strain rate, the fluid column undergoes a transition from a liquid-like breakup to a fracture mode, which we link to the dilatancy and jamming of the suspension. We also observe strong evidence of viscoelasticity in the liquid state close to this transition.


Strain-rate-dependent jamming transition

Figure 1 shows stretched samples of a suspension of volume fraction ϕ 0.603. At low strain rates, a conventional filament is formed, which thins until it eventually breaks. In contrast, at high strain rates we notice angular features, with the fluid column apparently composed of 'granular' macroscopic lumps. Abrupt fracture of this column is then observed, followed by separation of the two parts. After this, their angular features slowly relax, creating a pair of hemispherical droplets. For intermediate strain rates, we obtain a surprisingly complex interplay of these two types of behaviour: initially the fluid column behaves as though composed of granules, but before complete fracture occurs, a flowable filament is recovered. Supplementary movie 1 shows this for a suspension with ϕ 0.603 at an extension rate of 1.3 s−1.

Figure 1: Extension rate-dependent morphologies of a dense colloidal suspension.
figure 1

(a) At low strain rates, the colloidal solution (volume fraction 0.603) forms a filament that subsequently drains towards the end plates before undergoing capillary-induced breakup ('liquid'). At higher rates, the system jams and subsequently fractures ('jammed'). Intermediate strain rates yield an interesting composite of the two morphologies ('transition'). (b) Steady-state shear rheology of the same suspension, performed using stainless steel cone-plate geometry. Filled squares, strain-rate-controlled data; open triangle and open circle, stress-controlled data.

These results show that a colloidal suspension, with nearly hard-core particle interactions, can exhibit jamming and brittle fracture under tensile loading of a fluid column. To investigate this jamming transition further, we studied its dependence on volume fraction. Figure 2 shows that, when ϕ is altered by only a few percent, the critical strain rate shifts by two or three orders of magnitude. The insets illustrate the morphologies in the transitional regime at different volume fractions. One might expect equivalent behaviour to be seen for different volume fractions, at similar locations relative to the critical strain rate. However, qualitative differences are apparent: we see increasing asymmetry at high volume fraction ϕ (when suspensions often pull towards one edge of the rheometer) and also increasing lumpiness. The direction of symmetry breaking varies unsystematically from experiment to experiment (unrelated to loading and/or surfaces). The lack of symmetry becomes noticeable, as the granules get sufficiently large compared with the flow geometry, thus making the fluid structure non-uniform. These changes at high ϕ correlate with the onset of remarkable viscoelastic effects (recoil) to which we return below.

Figure 2: Volume fraction dependence of the extensional jamming transition.
figure 2

'Jammed' (open triangle), 'Transition' (filled square), 'Liquid' (open circle). Changes of a few percent in volume fraction result in a shift of the characteristic strain rate of the transition by orders of magnitude. The images highlight the dependence of the morphology at the transition on volume fraction (ϕ 0.588, 0.596 and 0.603). On increasing ϕ, both the granule size and general asymmetry of the paste structure increases. Similar trends are observed for the jammed state.

The shear contribution to thickening

To better-understand our results for jamming of repulsive colloids under tensile stress, we recall that, with linear plate separation, the flow of our suspensions has a significant shear component, whose importance may depend on the sample geometry, extension rate and volume fraction. In pure shear flow, dense hard-sphere suspensions typically exhibit marked thickening within the range of volume fractions studied here, and indeed, the ϕ dependence of the tensile jamming transition in Figure 2 is very similar to that of the shear-thickening transition reported in Frith et al.1 We therefore performed traditional shear rheology on our own samples (Fig. 1). For ϕ =0.603, the suspension is strongly shear thinning at shear rates <2 s−1, whereas higher shear rates produce strong thickening. (Our results do not rule out a weak yield stress at very low strain rates, which is not relevant to the experiments reported here.) Comparing the critical strain rate of 2 s−1 with the results for extension (Fig. 2), we find a good agreement. This supports the idea that the jamming transition in a colloidal fluid under tensile load, if not directly controlled by shear thickening, at least involves closely related physics.

Shear thickening in colloids can be hydrodynamically mediated, continuous and reversible3, but more typical for high-volume fractions is the rather sharp onset shown in Figure 2. This sudden thickening has been interpreted as stress-induced jamming6, in which an applied stress that might otherwise promote a flow instead induces dilatancy and thus, counterintuitively, prevents flow.

Role of dilatancy in jamming

To test the contribution of dilatancy to our jammed state, we imaged the fluid surface during stretching (Fig. 3, Supplementary movie 2). Dilatancy causes individual colloids to encounter the fluid–air interface, which, hence, is deformed and should undergo a macroscopic change from glossy to matt appearance6. We observe just such a change, concurrent with the onset of macroscopic lumpiness (granulation), in all our samples. This confirms the direct role of dilatancy in the granulation and subsequent fracture of colloidal suspensions under tensile loading. Although dilatancy has been observed in various shear-flow geometries5,6,12,13, its effects when stretching a fluid column appear particularly pronounced.

Figure 3: Dilatancy during the jamming of colloidal suspension.
figure 3

As the column of fluid is extended (volume fraction 0.603, extension rate 3.5 s−1), the glossy surface seen at equilibrium (a) becomes matt, as the suspending liquid retreats into the particle interstices (b). A combination of shear thickening and dilatancy lead to jamming, granulation and finally to fracture. The suspension then slowly relaxes back into the equilibrium phase (c, d).

In bulk suspensions, dilatancy at fixed volume fraction causes an increase in the non-equilibrium osmotic pressure (particle pressure), varying roughly as Π≈ηɛ /(1−(φ/φ0))2, where η is the viscosity and ɛ˙ the strain rate14. A simple quantitative estimate of the onset of granulation equates this to the Laplace pressure, σ/D, where σ is the surface tension and D the column diameter. With σ=0.03 N m−1 and η=0.004 Pa s, this gives a critical strain rate of order 10 s−1 at ϕ =0.6, and also accounts for the decreasing trend with ϕ seen in Figure 2.

Elastic recoil of self-filtering filament

Having noted the role of dilatancy in the jammed state, we now return to describe a remarkable feature of the concentrated 'liquid-like' state. When a colloidal filament is stretched at a rate below the critical strain rate, it slowly narrows as fluid drains towards the end plates. However, at ϕ ≥0.603 and when the filament is <100 μm across, we see evidence of strong viscoelasticity. The filament breaks in a superficially fluid-like manner, but then recoils (Fig. 4). This recoil is only observed for large ϕ and at strain rates close to the transition. For ϕ 0.603 and 0.612, there is an initial rapid recoil, which quickly slows. The full recoil takes 1 and 2.1 s, respectively, comparable with the respective relaxation time periods (Fig. 2). The presence of such a recoil indicates that our 'fluid-like' filament can in fact support a strong tensile stress—and does so elastically.

Figure 4: Viscoelasticity of colloidal filaments.
figure 4

(a) Despite the apparent viscous flow characterizing the thinning of the 'liquid state' filament, on rupture we observe a strong elastic recoil of the filament towards the top plate, and a subsequent slow relaxation of this thread into the fluid state. For ϕ 0.603 (pictured) recoil of the filament takes 1 s. Extension rate is 0.65 s−1. (b) The natural logarithm of the mean filament diameter (measured in three places) in microns as a function of time. The error bars represent the standard deviation of the filament diameter measurements. The filament thins exponentially with time, as would be expected for an Oldroyd-B fluid. Departure from this indicates the development of strong additional stresses caused by jamming. As the filament continues to be stretched, the diameter remains constant.

Analysis of the change in diameter (D) of the filament before breakage shows an exponential decrease with time, reminiscent of a conventional viscoelastic material such as an Oldroyd-B fluid15. However, Figure 4 shows that on the final approach to breakage and recoil, there is a significant departure from this behaviour, with the filament diameter remaining almost constant in time. This is the evidence for the development of enhanced resistance to flow of fluid out of the thinning neck13, which we take to indicate the onset of jamming.

In the experimental geometry, the filament undergoes not only tensile stretching from the moving plates but also drainage caused by surface tension15. This raises the possibility that, in our fluid-like samples, jamming just before breakage is caused by self-filtration5, that is, differential motion between particles and fluid in the thinning filament, so that the particles are left behind in the same place as the fluid drains away. As ϕ increases, the particles form a jammed bed of fixed diameter at the centre of the column. Further drainage leaves insufficient fluid to cover these particles. Stretching of this filament now requires work to be done against the capillary forces, creating a large tensile stress. This work is recoverable (elastic): when the filament breaks it recoils, releasing the stored interfacial energy. This picture implies subtle changes to the filament geometry, after jamming but before breakage, which cannot be fully resolved by our experiments. Moreover, a very similar sequence of events would be expected even if jamming were caused instead by conventional dilation, in response to a gradual increase of local flow rate during the experiment. However, such an increase would be at odds with our observations in the transitional regime wherein samples start jammed, but then become fluid.

Two simple quantitative estimates lend support to a self-filtration mechanism for the eventual jamming of very thin fluid-like filaments. First, jamming occurs when the filament diameter is of order 200 times the particle radius; this is comparable with the onset of self-filtration in other geometries4,5. Second, a radial pressure gradient estimated σ/D2, arising from the Laplace pressure, would—for a fluid cylinder not pinned to the particles—drive a radial flow velocity u(σ/D2) ka2/η, where k is a modified Carman-Kozeny coefficient, a is the particle radius, and ka2 = K is the permeability of the packed bed; for φ0.6 the geometrical constant k(φ) is estimated16 as 4×10−3. For D100 μm, this gives u1 μm s−1, leading to percent-scale changes in the fluid/particle volume ratio, which is enough to cause jamming, on a timescale of seconds. This argument mirrors the calculation of the radial flow velocity in a Newtonian fluid filament without particles16, which is recovered by setting KD2 instead.


In this study, we have investigated the flow behaviour of concentrated suspensions of nearly hard-sphere colloids under tensile loading. We showed that above a critical extension rate, the fluid jams and dilates, exhibiting dramatic granulation and subsequent fracture behaviour, closely related to shear-thickening and jamming in simple shear flow. We demonstrated that near this transition, even the flowable liquid displays surprising viscoelastic properties.

Simple estimates were given that account for the order of magnitude of the critical extension rate and its decreasing trend with volume fraction, and for the onset of a second, distinct, transition to jammed behaviour in very thin filaments before the final breakup. These estimates imply that the second transition, but not the first, is strongly dependent on the particle size. We leave experimental tests of this to future work.

Although our work aims primarily at elucidating the physical mechanisms governing dense colloidal suspensions subject to extensional deformations, it is directly relevant to a variety of practical applications in which a certain volume of colloidal suspension becomes separated from the rest, such as in dispensing the material through a narrow outlet or nozzle. (This situation arises in ink-jet technologies17,18, as well as in food and personal care products.) Indeed, the viscoelastic recoil of the filament that we observed just after breakup might cause nozzle clogging, with obvious consequences for operation. Moreover, the different breakup regimes observed in our experiments suggest that, in many practical cases, it will not be possible to control with precision the position where detachment occurs and hence the dispensed volume. We hope our study will promote further work on the physics of colloidal suspensions in flows, more complex than simple shear, that have significant implications for process control.


Sample preparation

Experiments were performed with poly(methyl methacrylate) spheres (radius a604 nm, 5% polydispersity) sterically stabilized by a chemically grafted poly-12-hydroxy stearic acid19 and suspended in octadecene, chosen because of its very low volatility. Refractive index matching is not as good as in some volatile solvents, but the residual inter-particle attraction remains very small20. Suspensions were centrifuged at 2,000 r.p.m. for 12 h to create a sediment. The volume fractions ϕ were produced by dilution of a stock solution, assuming ϕ0=0.640. (Our ϕ values are then quoted to the accuracy of the subsequent dilution.) Before use, and after each dilution, the particles were thoroughly mixed using a vortex whirlie mixer to ensure uniformity.

Extension measurements

Extension measurements were made using a HAAKE CaBER 1 Extensional Rheometer. It consists of two parallel cylindrical stainless steel plates, 6 mm in diameter and with an initial separation of 2 mm. Suspensions were loaded into the rheometer to form a cylindrical column between the two plates, either by using a spatula (ϕ >0.6) or using a 1 ml luer lock syringe (ϕ <0.6). In the latter case, solutions were drawn out and deposited slowly to prevent changes in the final volume fraction5. The plates are then separated at a constant velocity. All strain rates are quoted using the macroscopic separation of the end plates We note that this will, in general, be related in a highly non-linear way to the strain rate at different points in the sample, with a decreasing strain rate with increasing separation of the plates.

The stretching of the colloidal suspensions was observed using a high-speed camera (MC1311, Mikrotron) equipped with a Sony 18–108 mm/f2.5 zoom lens (Sony) and a 30 mm extension tube at frame rates from 50 to 500 f.p.s. Back illumination was provided by a 4 W Philips white light (Philips) viewed through a simple diffuser. However, for high-magnification imaging of the filament surface, the light-emitting diode was arranged so as to reflect back off the solution. The images were captured using a×2.5 zoom lens (Edmund Optics, VZM450i).

Shear rheology measurements

Shear rheology measurements were performed using a cone-plate rheometer, cone diameter 4 cm, cone angle 2°.

Additional information

How to cite this article: Smith, M.I. et al. Dilatancy in the flow and fracture of stretched colloidal suspensions. Nat. Commun. 1:114 doi: 10.1038/ncomms1119 (2010).


  1. Frith, W. J., d'Haene, P. & Buscall, R. Shear thickening in model suspensions of sterically stabilized particles. J. Rheol. 40, 531–548 (1996).

    ADS  CAS  Article  Google Scholar 

  2. Lootens, D., Damme, H. V. & Hebraud, P. Giant stress fluctuations at the jamming transition. Phys. Rev. Lett. 90, 178301 (2003).

    ADS  Article  Google Scholar 

  3. Maranzano, B. J. & Wagner, N. J. The effects of interparticle interactions and particle size on reversible shear thickening: hard-sphere colloidal dispersions. J. Rheol. 45, 1205–1222 (2001).

    ADS  CAS  Article  Google Scholar 

  4. Isa, L., Besseling, R., Morozov, A. N. & Poon, W. C. K. Velocity oscillations in microfluidic flows of concentrated colloidal suspensions. Phys. Rev. Lett. 102, 058302 (2009).

    ADS  Article  Google Scholar 

  5. Haw, M. D. Jamming, two-fluid behaviour, and 'Self-filtration' in concentrated particulate suspensions. Phys. Rev. Lett. 92, 185506 (2004).

    ADS  CAS  Article  Google Scholar 

  6. Cates, M. E., Haw, M. D. & Holmes, C. B. Dilatancy, jamming, and the physics of granulation. J Phys. Condens. Matter 17, S2517–S2531 (2005).

    ADS  CAS  Article  Google Scholar 

  7. Reynolds, O. On the dilatancy of media composed of rigid particles in contact. With experimental illustrations. Phil. Mag. 20 (Series 5), 469–481 (1885).

    Article  Google Scholar 

  8. Rodd, L. E., Scott, T. P., Cooper-White, J. J. & McKinley, G. H. Capillary break-up rheometry of low-viscosity elastic fluids. Appl. Rheol. 15, 12–27 (2005).

    CAS  Google Scholar 

  9. Mckinley, G. H. & Sridhar, T. Filament stretching rheometry of complex fluids. Annu. Rev. Fluid. Mech. 34, 375–415 (2002).

    ADS  MathSciNet  Article  Google Scholar 

  10. Bischoff White, E. E., Chellamuthu, M. & Rothstein, J. P. Extensional rheology of a shear-thickening cornstarch and water suspension. Rheol. Acta. 49, 119–129 (2010).

    CAS  Article  Google Scholar 

  11. Chellamuthu, M., Arndt, E. M. & Rothstein, J. P. Extensional rheology of shear-thickening nanoparticle suspensions. Soft Matter 5, 2117–2124 (2009).

    ADS  CAS  Article  Google Scholar 

  12. Fall, A., Huang, N., Bertrand, F., Ovarlez, G. & Bonn, D. Shear thickening of cornstarch suspensions as a reentrant jamming transition. Phys. Rev. Lett. 100, 018301 (2008).

    ADS  Article  Google Scholar 

  13. Larsen, R. J., Kim, J., Zukoski, C. F. & Weitz, D. A. Elasticity of dilatant particle suspensions during flow. Phys. Rev. E 81, 011502 (2010).

    ADS  Article  Google Scholar 

  14. Morris, J. F. & Boulay, F. Curvilinear flows of noncolloidal suspensions: the role of normal stresses. J. Rheol. 43, 1213 (1999).

    ADS  CAS  Article  Google Scholar 

  15. Anna, S. L. & McKinley, G. H. Elasto-capillary thinning and breakup of model elastic liquids. J. Rheol. 45, 115 (2001).

    ADS  CAS  Article  Google Scholar 

  16. Dufresne, E. R. et al. Flow and fracture in drying nanoparticle suspensions. Phys. Rev. Lett. 91, 224501 (2003).

    ADS  CAS  Article  Google Scholar 

  17. Lewis, J. A. Colloidal processing of ceramics. J. Am. Ceram. Soc. 83, 2341–59 (2000).

    CAS  Article  Google Scholar 

  18. Lewis, J. A. Direct-write assembly of ceramics from colloidal inks. Curr. Opin. Solid State Mater. Sci. 6, 245–250 (2002).

    ADS  CAS  Article  Google Scholar 

  19. Antl, L. et al. The preparation of poly(methyl-methacrylate) latices in non-aqueous media. Colloids Surf. 17, 67–78 (1986).

    CAS  Article  Google Scholar 

  20. Koumakis, N., Schofield, A. B. & Petekidis, G. Effect of shear induced crystallization on the rheology and aging of hard sphere glasses. Soft Matter 4, 2008–2018 (2008).

    ADS  CAS  Article  Google Scholar 

  21. Eggers, J. & Villermaux, E. Physics of liquid jets. Rep. Prog. Phys. 71, 026601 (2008).

    Article  Google Scholar 

  22. Larson, R. G. The Structure and Rheology of Complex Fluids (Oxford University Press, 1999).

Download references


We thank Andrew Schofield for particle synthesis. The work was funded by the UK EPSRC (Grant nos EP/E03173/1 and EP/E005950/1). M.E.C. holds a Royal Society Research Professorship. V.B. acknowledges a Visiting Professor Fellowship from Politecnico di Torino-Regione Piemonte.

Author information

Authors and Affiliations



M.I.S. performed the extensional rheology measurements, R.B. performed the shear rheology measurements. All authors contributed to the interpretation and discussion of results, and to the drafting of the manuscript.

Corresponding author

Correspondence to V. Bertola.

Ethics declarations

Competing interests

The authors declare no competing financial interests.

Supplementary information

Supplementary Movie 1

Stretching of a colloidal suspension (phi = 0.603) at an extension rate of 1.3 s-1. Whilst granulation may be observed at the beginning of stretching, a flowable liquid filament is recovered before breakup. (AVI 1864 kb)

Supplementary Movie 2

Stretching of a colloidal suspension (phi = 0.603) at an extension rate of 3.5 s-1. Dilatancy causes the surface to change from glossy to matt appearance. (AVI 2453 kb)

Rights and permissions

Reprints and Permissions

About this article

Cite this article

Smith, M., Besseling, R., Cates, M. et al. Dilatancy in the flow and fracture of stretched colloidal suspensions. Nat Commun 1, 114 (2010).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI:

Further reading


By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.


Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing