The mixing of polymers and nanoparticles is opening pathways for engineering flexible composites that exhibit advantageous electrical, optical, or mechanical properties. Recent advances reveal routes to exploit both enthalpic and entropic interactions so as to direct the spatial distribution of nanoparticles and thereby control the macroscopic performance of the material. For example, by tailoring the particle coating and size, researchers have created self-healing materials for improved sustainability and self-corralling rods for photovoltaic applications. A challenge for future studies is to create hierarchically structured composites in which each sublayer contributes a distinct function to yield a mechanically integrated, multifunctional material.

http://science.sciencemag.org/content/sci/314/5802/1107.full.pdf

Nanoparticle Polymer Composites: Where Two Small Worlds Meet

Nanotechnology is being used to enhance conventional ceramic and polymeric water treatment membrane materials through various avenues. Among the numerous concepts proposed, the most promising to date include zeolitic and catalytic nanoparticle coated ceramic membranes, hybrid inorganic–organic nanocomposite membranes, and bio-inspired membranes such as hybrid protein–polymer biomimetic membranes, aligned nanotube membranes, and isoporous block copolymer membranes. A semi-quantitative ranking system was proposed considering projected performance enhancement (over state-of-the-art analogs) and state of commercial readiness. Performance enhancement was based on water permeability, solute selectivity, and operational robustness, while commercial readiness was based on known or anticipated material costs, scalability (for large scale water treatment applications), and compatibility with existing manufacturing infrastructure. Overall, bio-inspired membranes are farthest from commercial reality, but offer the most promise for performance enhancements; however, nanocomposite membranes offering significant performance enhancements are already commercially available. Zeolitic and catalytic membranes appear reasonably far from commercial reality and offer small to moderate performance enhancements. The ranking of each membrane nanotechnology is discussed along with the key commercialization hurdles for each membrane nanotechnology.

/pdf/a-review-of-water-treatment-membrane-nanotechnologies-1np07if946.pdf

A review of water treatment membrane nanotechnologies

Lattice-gas cellular automata (LGCA) and lattice Boltzmann models (LBM) are relatively new andpromising methods for the numerical solution of nonlinear partial differential equations. The bookprovides an introduction for graduate students and researchers. Working knowledge of calculus isrequired and experience in PDEs and fluid dynamics is recommended. Some peculiarities of cellularautomata are outlined in Chapter 2. The properties of various LGCA and special coding techniquesare discussed in Chapter 3. Concepts from statistical mechanics (Chapter 4) provide the necessarytheoretical background for LGCA and LBM. The properties of lattice Boltzmann models and amethod for their construction are presented in Chapter 5.

/pdf/lattice-gas-cellular-automata-and-lattice-boltzmann-models-2kkc77jjx8.pdf

Lattice-Gas Cellular Automata and Lattice Boltzmann Models

Recent advances in the stabilization of emulsions and foams by particles of nanoscale and microscopic dimensions are described. Ongoing research in this highly active field is providing insight into (i) the molecular factors controlling particle wettability and adsorption, (ii) the structural and mechanical properties of particle-laden liquid interfaces, and (ii) the stabilization mechanisms of particle-coated droplets and bubbles. There is much potential for exploiting the emerging knowledge in new food product applications. The preparation of cheap and effective colloidal particles based on food-grade ingredients, especially proteins, is the key technological challenge.

Food emulsions and foams: Stabilization by particles

Templating is one of the most important techniques for the controlled synthesis of nanostructured materials. This powerful tool uses a pre-existing guide with desired nanoscale features to direct the formation of nanomaterials into forms that are otherwise difficult to obtain. As a result, templated synthesis is capable of producing nanostructures with unique structures, morphologies and properties. In this review, we summarize the general principles of templated synthesis and cover recent developments in this area. As a wide variety of synthesis techniques are utilized to produce nanomaterials using template-based methods, the discussion is organized around the various types of common templates. We examine the use of both physical and chemical hard colloidal templates, soft templates, and other non-colloidal templates, followed by our perspective on the state of the field and potential future directions.

Templated synthesis of nanostructured materials

Colloidal particles or nanoparticles, with equal affinity for two fluids, are known to adsorb irreversibly to the fluid-fluid interface. We present large-scale computer simulations of the demixing of a binary solvent containing such particles. The newly formed interface sequesters the colloidal particles; as the interface coarsens, the particles are forced into close contact by interfacial tension. Coarsening is markedly curtailed, and the jammed colloidal layer seemingly enters a glassy state, creating a multiply connected, solidlike film in three dimensions. The resulting gel contains percolating domains of both fluids, with possible uses as, for example, a microreaction medium.

https://arxiv.org/pdf/cond-mat/0510040.pdf

Colloidal jamming at interfaces: a route to fluid-bicontinuous gels.

The late-stage demixing following spinodal decomposition of a three-dimensional symmetric binary fluid mixture is studied numerically, using a thermodynamically consistent lattice Boltzmann method. We combine results from simulations with different numerical parameters to obtain an unprecedented range of length and time scales when expressed in reduced physical units. (These are the length and time units derived from fluid density, viscosity, and interfacial tension.) Using eight large (2563) runs, the resulting composite graph of reduced domain size l against reduced time t covers 1 [less, similar] l [less, similar] 105, 10 [less, similar] t [less, similar] 108. Our data are consistent with the dynamical scaling hypothesis that l(t) is a universal scaling curve. We give the first detailed statistical analysis of fluid motion, rather than just domain evolution, in simulations of this kind, and introduce scaling plots for several quantities derived from the fluid velocity and velocity gradient fields. Using the conventional definition of Reynolds number for this problem, Reφ = ldl/dt, we attain values approaching 350. At Reφ [greater, similar] 100 (which requires t [greater, similar] 106) we find clear evidence of Furukawa's inertial scaling (l [similar] t2/3), although the crossover from the viscous regime (l [similar] t) is both broad and late (102 [less, similar] t [less, similar] 106). Though it cannot be ruled out, we find no indication that Reφ is self-limiting (l [similar] t1/2) at late times, as recently proposed by Grant & Elder. Detailed study of the velocity fields confirms that, for our most inertial runs, the RMS ratio of nonlinear to viscous terms in the Navier-Stokes equation, R2, is of order 10, with the fluid mixture showing incipient turbulent characteristics. However, we cannot go far enough into the inertial regime to obtain a clear length separation of domain size, Taylor microscale, and Kolmogorov scale, as would be needed to test a recent 'extended' scaling theory of Kendon (in which R2 is self-limiting but Reφ not). Obtaining our results has required careful steering of several numerical control parameters so as to maintain adequate algorithmic stability, efficiency and isotropy, while eliminating unwanted residual diffusion. (We argue that the latter affects some studies in the literature which report l [similar] t2/3 for t [less, similar] 104.) We analyse the various sources of error and find them just within acceptable levels (a few percent each) in most of our datasets. To bring these under significantly better control, or to go much further into the inertial regime, would require much larger computational resources and/or a breakthrough in algorithm design.

/pdf/inertial-effects-in-three-dimensional-spinodal-decomposition-3lu8ilsmv9.pdf

Inertial effects in three-dimensional spinodal decomposition of a symmetric binary fluid mixture: a lattice Boltzmann study

LUDWIG: A parallel Lattice-Boltzmann code for complex fluids

We simulate late-stage coarsening of a 3D symmetric binary fluid using a lattice Boltzmann method. With reduced lengths and times, $l$ and $t$, respectively (with scales set by viscosity, density, and surface tension), our data sets cover $1\ensuremath{\lesssim}l\ensuremath{\lesssim}{10}^{5}$ and $10\ensuremath{\lesssim}t\ensuremath{\lesssim}{10}^{8}$. We achieve Reynolds numbers approaching $350$. At $\mathrm{Re}\ensuremath{\gtrsim}100$ we find clear evidence of Furukawa's inertial scaling ( $l\ensuremath{\sim}{t}^{2/3}$), although the crossover from the viscous regime ( $l\ensuremath{\sim}t$) is very broad. Though it cannot be ruled out, we find no indication that Re is self-limiting ( $l\ensuremath{\sim}{t}^{1/2}$) as proposed by M. Grant and K. R. Elder [Phys. Rev. Lett. 82, 14 (1999)].

https://arxiv.org/pdf/cond-mat/9902346.pdf

3D spinodal decomposition in the inertial regime

We present a progress report on our work on lattice Boltzmann methods for colloidal suspensions. We focus on the treatment of colloidal particles in binary solvents and on the inclusion of thermal noise. For a benchmark problem of colloids sedimenting and becoming trapped by capillary forces at a horizontal interface between two fluids, we discuss the criteria for parameter selection, and address the inevitable compromise between computational resources and simulation accuracy.

https://iopscience.iop.org/article/10.1088/0953-8984/16/38/009/pdf

J. C. Desplat

Papers

Colloidal jamming at interfaces: a route to fluid-bicontinuous gels.

Inertial effects in three-dimensional spinodal decomposition of a symmetric binary fluid mixture: a lattice Boltzmann study

LUDWIG: A parallel Lattice-Boltzmann code for complex fluids

3D spinodal decomposition in the inertial regime

Simulating colloid hydrodynamics with lattice Boltzmann methods