Droplet microfluidics generates and manipulates discrete droplets through immiscible multiphase flows inside microchannels Due to its remarkable advantages, droplet microfluidics bears significant value in an extremely wide range of area In this review, we provide a comprehensive and in-depth insight into droplet microfluidics, covering fundamental research from microfluidic chip fabrication and droplet generation to the applications of droplets in bio(chemical) analysis and materials generation The purpose of this review is to convey the fundamentals of droplet microfluidics, a critical analysis on its current status and challenges, and opinions on its future development We believe this review will promote communications among biology, chemistry, physics, and materials science

Emerging Droplet Microfluidics

Surfactants And Interfacial Phenomena

Droplet microfluidics offers exquisite control over the flows of multiple fluids in microscale, enabling fabrication of advanced microparticles with precisely tunable structures and compositions in a high throughput manner The combination of these remarkable features with proper materials and fabrication methods has enabled high efficiency, direct encapsulation of actives in microparticles whose features and functionalities can be well controlled These microparticles have great potential in a wide range of bio-related applications including drug delivery, cell-laden matrices, biosensors and even as artificial cells In this review, we briefly summarize the materials, fabrication methods, and microparticle structures produced with droplet microfluidics We also provide a comprehensive overview of their recent uses in biomedical applications Finally, we discuss the existing challenges and perspectives to promote the future development of these engineered microparticles

/pdf/microfluidic-fabrication-of-microparticles-for-biomedical-2tsrw0ufu5.pdf

Microfluidic fabrication of microparticles for biomedical applications

Advances in application of ultrasound in food processing: A review.

We carry out numerical simulations to study transport behavior about the jamming transition of a model granular material in two dimensions at zero temperature. Shear viscosity eta is computed as a function of particle volume density rho and applied shear stress sigma, for diffusively moving particles with a soft core interaction. We find an excellent scaling collapse of our data as a function of the scaling variable sigma/|rho(c)-rho|(Delta), where rho(c) is the critical density at sigma=0 ("point J"), and Delta is the crossover scaling critical exponent. We define a correlation length xi from velocity correlations in the driven steady state and show that it diverges at point J. Our results support the assertion that jamming is a true second-order critical phenomenon.

http://absimage.aps.org/image/MAR09/MWS_MAR09-2008-006918.pdf

Critical Scaling of Shear Viscosity At the Jamming Transition

We report a small angle neutron scattering (SANS) and rheology study of cellulose derivative polyelectrolyte sodium carboxymethyl cellulose with a degree of substitution of 1.2. Using SANS, we establish that this polymer is molecularly dissolved in water with a locally stiff conformation with a stretching parameter[Formula: see text]. We determine the cross sectional radius of the chain ([Formula: see text] 3.4 A) and the scaling of the correlation length with concentration (ξ = 296 c (-1/2)A for c in g/L) is found to remain unchanged from the semidilute to concentrated crossover as identified by rheology. Viscosity measurements are found to be in qualitative agreement with scaling theory predictions for flexible polyelectrolytes exhibiting semidilute unentangled and entangled regimes, followed by what appears to be a crossover to neutral polymer concentration dependence of viscosity at high concentrations. Yet those higher concentrations, in the concentrated regime defined by rheology, still exhibit a peak in the scattering function that indicates a correlation length that continues to scale as[Formula: see text]. © 2014 The Authors. Journal of Polymer Science Part B: Polymer Physics Published by Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2015, 53, 492-501.

https://www.onlinelibrary.wiley.com/doi/pdf/10.1002/polb.23657

Structure of sodium carboxymethyl cellulose aqueous solutions: A SANS and rheology study

The swelling of thermoresponsive microgels is widely modelled through Flory–Rehner theory, which combines Flory–Huggins solution thermodynamics with the affine network model of elasticity. While it has been shown that FR theory closely follows experimental results for a range of systems, the large number of free parameters required to fit size vs. temperature data make a proper evaluation of the theory difficult. In order to test the applicability of FR theory to microgel particles, we analyse viscosity and light scattering data for PNIPAM microgels as a function of temperature, cross-linking degree (f) and molar mass. In the collapsed state, the polymer volume fraction is estimated to be ϕC ≃ 0.44, independent of cross linking degree and molar mass. Fixing ϕC, f and the θ temperature to independent estimates, the FR model appears to describe microgel swelling well, particularly for high cross-linking densities. Estimates for the various fit parameters differ from earlier reports by an order of magnitude. A comparison of the χ parameter obtained from FR theory with values for the linear polymer reveals that the agreement between experiment and theory is somewhat fortuitous. Although the FR model can accurately describe experimental data, the accuracy of the obtained fit parameters is significantly poorer.

Does Flory-Rehner theory quantitatively describe the swelling of thermoresponsive microgels?

We investigate the viscosity dependence on concentration and molecular weight of semiflexible polyelectrolyte sodium carboxymethylcellulose (NaCMC) in aqueous salt-free and NaCl solutions. Combining new measurements and extensive literature data, we establish relevant power laws and crossovers over a wide range of degree of polymerization (N) as well as polymer (c) and salt (cs) concentrations. In salt-free solution, the overlap concentration shows the expected c* ∝ N–2 dependence, and the entanglement crossover scales as ce ∝ N–0.6±0.3, in strong disagreement with scaling theory for which ce ∝ c* is expected, but matching the behavior found for flexible polyelectrolytes. A second crossover, to a steep concentration dependence for specific viscosity (ηsp ∝ c3.5±0.2), commonly assigned to the concentrated regime, is shown to follow c** ∝ N–0.6±0.2 (with c**/ce ≃ 6) which thus suggests instead a dynamic crossover, possibly related to entanglement. The scaling of c* and ce in 0.01 and 0.1 M NaCl shows neutra...

/pdf/viscosity-and-scaling-of-semiflexible-polyelectrolyte-nacmc-4nzq70blay.pdf

Viscosity and Scaling of Semiflexible Polyelectrolyte NaCMC in Aqueous Salt Solutions

The rheology of water-soluble polyelectrolytes at intermediate and high concentrations is controlled by entanglement, hydrophobic, and electrostatic interactions, whose influences are difficult to isolate. We investigate the rheology of semidilute solutions of sodium carboxymethyl cellulose (NaCMC) with molecular weight Mw ≃ 2.5 × 105 g/mol and varying degree of substitution (DS) as a function of polymer concentration in various solvent media: salt-free water (long-ranged electrostatic interactions), 0.5 M aqueous NaCl (screened electrostatics), and 0.5 M aqueous NaOH (screened electrostatics, diminished hydrophobic interactions) in order to selectively examine the role played by these different interactions. Decreasing DS is found to decrease solubility and induce partial aggregation and eventual gelation. In salt-free and 0.5 M NaCl solution, NaCMC with DS ≃ 1.2 exhibits hydrophilic polyelectrolyte and neutral polymer in good solvent behavior, respectively. Decreasing DS to ≃0.7–0.8 leads to hydrophobic...

Carlos G. Lopez

Papers

Structure of sodium carboxymethyl cellulose aqueous solutions: A SANS and rheology study

Does Flory-Rehner theory quantitatively describe the swelling of thermoresponsive microgels?

Viscosity and Scaling of Semiflexible Polyelectrolyte NaCMC in Aqueous Salt Solutions

Electrostatic and Hydrophobic Interactions in NaCMC Aqueous Solutions: Effect of Degree of Substitution

Electrostatic and hydrophobic interactions in NaCMC aqueous solutions: effect of degree of substitution and solvent medium on structure and rheology.