Versatile Aerogel Fabrication by Freezing and Subsequent Freeze‐Drying of Colloidal Nanoparticle Solutions

A versatile method to fabricate self‐supported aerogels of nanoparticle (NP) building blocks is presented. This approach is based on freezing colloidal NPs and subsequent freeze drying. This means that the colloidal NPs are directly transferred into dry aerogel‐like monolithic superstructures without previous lyogelation as would be the case for conventional aerogel and cryogel fabrication methods. The assembly process, based on a physical concept, is highly versatile: cryogelation is applicable for noble metal, metal oxide, and semiconductor NPs, and no impact of the surface chemistry or NP shape on the resulting morphology is observed. Under optimized conditions the shape and volume of the liquid equal those of the resulting aerogels. Also, we show that thin and homogeneous films of the material can be obtained. Furthermore, the physical properties of the aerogels are discussed.     

Superior Lithium‐Ion Storage Properties of Mesoporous CuO–Reduced Graphene Oxide Composite Powder Prepared by a Two‐Step Spray‐Drying Process

Mesoporous CuO–reduced graphene oxide (rGO) composite powders were prepared by using a two‐step spray‐drying process. In the first step, hollow CuO powders were prepared from a spray solution of copper nitrate trihydrate with citric acid and were wet milled to obtain a colloidal spray solution. In the second step, spray drying of the colloidal solution that contained dispersed GO nanosheets produced mesoporous CuO–rGO composite powders with particle sizes of several microns. Thermal reduction of GO nanosheets to rGO nanosheets occurred during post‐treatment at 300 °C. Initial discharge capacities of the hollow CuO, bare CuO aggregate, and CuO–rGO composite powders at a current density of 2 A g^?1 were 838, 1145, and 1238 mA h g^?1, respectively. Their discharge capacities after 200 cycles were 259, 380, and 676 mA h g^?1, respectively, and their corresponding capacity retentions measured from the second cycle were 67, 48, and 76 %, respectively. The mesoporous CuO–rGO composite powders have high structural stability and high conductivity because of the rGO nanosheets, and display good cycling and rate performances.     

Long‐term stability of an ambient self‐curable latex based on colloidal dispersions in water of two reactive polymers

An ambient self‐curable latex (ASCL) was prepared via the blending of colloidal dispersions in water of a chloromethylstyrene‐functionalized copolymer and a tertiary‐amine‐functionalized copolymer. Upon casting and drying under ambient conditions, the ASCL could generate crosslinked continuous polymer films. The crosslinking occurred via the Menschutkin reaction (quaternization) between the two types of functional groups. Because this reaction was reversible at high temperatures, the films could be decrosslinked and hence were self‐curable. The prepared ASCL exhibited excellent colloidal and chemical stability during long‐term storage: no significant changes in the colloidal properties, such as the particle size, electrophoretic mobility, and crosslinking reactivity, were observed after 48 months of storage. The electrophoretic measurements indicated that the electrostatic repulsion between the negatively charged particles of the ASCL was responsible for the excellent stability. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 2598–2605, 2005     

Dynamic self-assembly of polymer colloids to form linear patterns

A dynamic self-assembling process is reported which involves drying a droplet of positively charged colloidal suspension on a flat negatively charged hydrophilic surface. This extremely simple method affords lines of colloidal particles with regular 1.5-4.5 microm line spacing and smaller than 2 microm line width over a broad surface area. The ordered region diffracts light to display an iridescent appearance and generates first-order diffraction spots when illuminated by a He-Ne laser. A periodic stick-slip motion of the drying liquid front is observed during the drying process using optical microscopy. The periodic motion must be related to the periodic particle deposition. We propose that the simultaneous deposition of the particles at a fixed distance (i.e., the line spacing) behind the previous line of particles where the contact line is pinned is in turn responsible for the periodic stick-slip motion. The key distinguishing feature of the present system is the attractive interaction between the particles and the surface, which instigates the periodicity of the particle deposition.     

Colloidal transport phenomena of milk components during convective droplet drying

Material segregation has been reported for industrial spray-dried milk powders, which indicates potential material migration during drying process. The relevant colloidal transport phenomenon and the underlying mechanism are still under debate. This study extended the glass-filament single droplet drying technique to observe not only the drying behaviour but also the dissolution behaviour of the correspondingly dried single particle. At progressively longer drying stage, a solvent droplet (water or ethanol) was attached to the semi-dried milk particle and the interaction between the solvent and the particle was video-recorded. Based on the different dissolution and wetting behaviours observed, material migration during milk drying was studied. Fresh skim milk and fresh whole milk were investigated using water and ethanol as solvents. Fat started to accumulate on the surface as soon as drying was started. At the initial stage of drying, the fat layer remained thin and the solubility of the semi-dried milk particle was much affected by lactose and protein present underneath the fat layer. Fat kept accumulating at the surface as drying progressed and the accumulation was completed by the middle stage of drying. The results from drying of model milk materials (pure sodium caseinate solution and lactose/sodium caseinate mixed solution) supported the colloidal transport phenomena observed for the milk drying. When mixed with lactose, sodium caseinate did not form an apparent solvent-resistant protein shell during drying. The extended technique of glass-filament single droplet approach provides a powerful tool in examining the solubility of individual particle after drying.     

Sedimentation and drying dissipative patterns of binary suspensions of colloidal silica spheres having different sizes

The sedimentation and drying dissipative structural patterns were formed during the course of drying binary mixtures among colloidal silica spheres of 183 nm, 305 nm, and 1.205 μm in diameter in aqueous suspension on a watch glass, a glass dish, and a cover glass, respectively. The broad ring-like sedimentation patterns were formed within several hours in suspension state for all the substrates used. Colorful macroscopic broad ring-like drying patterns were formed for the three substrates. In a watch glass, macroscopic drying patterns were composed of the outer and inner layers of small and large spheres, respectively. The two colored layers were ascribed to the Bragg diffractions of light by the dried colloidal crystals of the corresponding spheres. The width ratio of the layers changed in proportion to the mixing ratio of each spheres. In a glass dish, wave-like macroscopic drying patterns were observed in the intermediate areas between the outside edges of the broad ring and the inner wall of the cell. On a cover glass, the sphere mixing ratios were analyzed from the widths of the drying broad rings of the small spheres at the outside edge. High and distinct broad rings of small spheres and the low and vague broad one formed at the outer edges and in the inner area, respectively. Drying dissipative pattern was clarified to be one of the novel analysis techniques of colloidal size in binary colloidal mixtures.     

Hafnia ceramic nanofiltration membranes. Part I: Preparation and characterization

We have used a sol–gel process as an efficient method for the preparation of hafnia nanofiltration membranes. A stable colloidal sol was obtained after hydrolysis of an alkoxide and peptization of the hydrous oxide precipitate. After the drying of the sol, the hafnia powder was characterized using several methods, such as X-ray diffraction, dilatometry, thermal analysis, electrophoretic, and BET measurements. The hafnia membrane was obtained by coating the colloidal sol on a mesoporous ceramic support, followed by a drying and sintering of the gelled layer. The membrane was characterized by SEM and nitrogen adsorption–desorption to determine the pore size. The filtration properties of a hafnia membrane sintered at 450°C were determined using water permeability and rejection of solutions containing sucrose, polyethylene glycols of different molecular weights (400, 600, 1000) and salt solutions. This membrane is characterized by a MWCO of 420 Da and pore size near 1 nm.     

Evolution of interparticle capillary forces during drying of colloidal crystals

Photonic crystals are periodic structures that have the capability to manipulate the photons in the same way as semiconductors do for electrons. The self-assembly strategy that utilizes colloidal crystals as a template to form photonic crystals has received a great deal of recent research interest because it is simple and cost-effective. Experimental studies and theoretical analysis have speculated that capillary forces play a pivotal role in forming the colloidal crystals during the crystal growth process and that particularly during the drying stage the changing of the magnitude of capillary forces is critical to the resultant microstructure. This paper presents a computational analysis of the changing capillary forces, which may throw light on a refined strategy for controlling colloidal crystal growth.     

Drying of a cellulose II gel: effect of physical modification and redispersibility in water

The agglomeration of cellulosic materials upon drying, often called hornification, causes a reduction of water retention, among other undesired effects. It is one of the main issues in industrial cellulose processing, especially with regard to nanocelluloses. As a consequence, high transportation and storage costs arise since nanocelluloses need to remain in aqueous suspensions unless trade-offs in reactivity, redispersibility and surface properties are accepted. In this study, different drying strategies for TENCEL^® gel, a nanostructured gel derived from the Lyocell process consisting of spherical particles, are compared and evaluated. First, freeze-drying with consideration of the influence of freezing temperature and the use of tert-butanol as cryo-protectant, and second, simple oven-drying at 60 °C. Surprisingly, oven-dried xerogels showed higher water retention values and also better colloidal stability than the cryogels. This is in stark contrast to cellulose nanofibrils for which freeze-drying has been shown to be significantly superior to oven drying in terms of redispersibility. For the TENCEL^® gel, oven-drying was thus selected and the influence of additives on the redispersibility of the cellulose II gel was studied by means of the common water retention value, particle size, colloidal stability, appearance of the redispersed gel and viscosity. The addition of the polysaccharides carboxymethyl cellulose or xanthan showed the most promising results with regard to redispersibility. Also sucrose and ammonium bicarbonate provided higher colloidal stabilities than that of the untreated TENCEL^® gel. The redispersibility of the cellulose II xerogels could thus be significantly improved by simple and cost-efficient mixing with additives prior to drying.     

Nanostructure and irreversible colloidal behavior of Ca(OH)2: implications in cultural heritage conservation

Although Ca(OH)2 is one of the oldest art and building material used by mankind, little is known about its nanostructural and colloidal characteristics that play a crucial role in its ultimate performance as a binder in lime mortars and plasters. In particular, it is unknown why hydrated lime putty behaves as an irreversible colloid once dried. Such effect dramatically affects the reactivity and rheology of hydrated lime dispersions. Here we show that the irreversible colloidal behavior of Ca(OH)2 dispersions is the result of an oriented aggregation mechanism triggered by drying. Kinetic stability and particle size distribution analysis of oven-dried slaked lime or commercial dry hydrate dispersions exhibit a significant increase in settling speed and particle (cluster) size in comparison to slaked lime putty that has never been dried. Drying-related particle aggregation also leads to a significant reduction in surface area. Electron microscopy analyses show porous, randomly oriented, micron-sized clusters that are dominant in the dispersions both before and after drying. However, oriented aggregation of the primary Ca(OH)2 nanocrystals (approximately 60 nm in size) is also observed. Oriented aggregation occurs both before and during drying, and although limited before drying, it is extensive during drying. Nanocrystals self-assemble in a crystallographically oriented manner either along the 100 or equivalent 110 directions, or along the Ca(OH)2 basal planes, i.e., along [001]. While random aggregation appears to be reversible, oriented aggregation is not. The strong coherent bonding among oriented nanoparticles prevents disaggregation upon redispersion in water. The observed irreversible colloidal behavior associated with drying of Ca(OH)2 dispersions has important implications in heritage conservation, particularly considering that nowadays hydrated lime is often the preferred alternative to portland cement in architectural heritage conservation. Finally, our study demonstrates that, fortuitously, hydrated lime could be one of the first nanomaterials used by mankind.     

Hollow‐Core Magnetic Colloidal Nanocrystal Clusters with Ligand‐Exchanged Surface Modification as Delivery Vehicles for Targeted and Stimuli‐Responsive Drug Release

The fabrication of hierarchical magnetic nanomaterials with well‐defined structure, high magnetic response, excellent colloidal stability, and biocompatibility is highly sought after for drug‐delivery systems. Herein, a new kind of hollow‐core magnetic colloidal nanocrystal cluster (HMCNC) with porous shell and tunable hollow chamber is synthesized by a one‐pot solvothermal process. Its novelty lies in the “tunability” of the hollow chamber and of the pore structure within the shell through controlled feeding of sodium citrate and water, respectively. Furthermore, by using the ligand‐exchange method, folate‐modified poly(acrylic acid) was immobilized on the surface of HMCNCs to create folate‐targeted HMCNCs (folate‐HMCNCs), which endowed them with excellent colloidal stability, pH sensitivity, and, more importantly, folate receptor‐targeting ability. These assemblages exhibited excellent colloidal stability in plasma solution. Doxorubicin (DOX), as a model anticancer agent, was loaded within the hollow core of these folate‐HMCNCs (folate‐HMCNCs‐DOX), and drug‐release experiments proved that the folate‐HMCNCs‐DOX demonstrated pH‐dependent release behavior. The folate‐HMCNCs‐DOX assemblages also exhibited higher potent cytotoxicity to HeLa cells than free doxorubicin. Moreover, folate‐HMCNCs‐DOX showed rapid cell uptake apart from the enhanced cytotoxicity to HeLa cells. Experimental results confirmed that the synthesized folate‐HMCNCs are smart nanovehicles as a result of their improved folate receptor‐targeting abilities and also because of their combined pH‐ and magnetic‐stimuli response for applications in drug delivery.     

CdSe Nanoplatelets: Living Polymers

Colloidal CdSe nanoplatelets are considered to be excellent candidates for many applications in nanotechnology. One of the current challenges is to self‐assemble these colloidal quantum wells into large ordered structures to control their collective optical properties. We describe a simple and robust procedure to achieve controlled face‐to‐face self‐assembly of CdSe nanoplatelets into micron‐long polymer‐like threads made of up to ～1000 particles. These structures are formed by addition of oleic acid to a stable colloidal dispersion of platelets, followed by slow drying and re‐dispersion. We could control the average length of the CdSe nanoplatelet threads by varying the amount of added oleic acid. These 1‐dimensional structures are flexible and feature a “living polymer” character because threads of a given length can be further grown through the addition of supplementary nanoplatelets at their reactive ends.     

Alternating crack propagation during directional drying

The propagation of fractures during the drying of a colloidal silica suspension confined in a vertical microtube is investigated. During the drying process, the particle concentration increases until gel formation. In the gelled region, the tensile stresses increase and lead to the formation of two vertical perpendicular cracks propagating in the drying direction, dividing the tube into four equivalent regions. Throughout the drying process, these two fractures do not propagate at the same velocity. The top crack inhibits the propagation of the crack that is left behind, and the slow propagation of a fracture is followed by the rapid propagation of the other.     

Formation and drying of colloidal crystals using nanosized silica particles

Much interest has been generated in the fabrication of colloidal crystals from suspensions because of the promise of photonic band gap applications. However, since the case of small, nonsedimenting colloidal particles indeed remains rather rarely treated, spherical silica particles with diameters varying from 75 down to 20 nm have been used in the present work to fabricate colloidal crystals by drying the suspending liquid. Typical events that take place during the drying process of a particulate film, such as cracking, compaction and penetration of air into a porous network, have been evaluated using existing theories, and the maximum stress in the drying film could be approximated. Investigation on the dry film structure by scanning electron microscopy showed the arrangement of particles in a close-packed system. To interpret the formation of such crystals, the amplitudes of the interparticle and capillary forces have been estimated from existing models. The repulsive interparticle forces allow the particles to remain stable and thus rearrange up to fairly high particle concentration. These modeling results showed the dominance of the capillary contribution at the end of the drying process. Nitrogen adsorption/desorption measurements gave very coherent results regarding both pore volume and pore size of the dry particulate films when compared to the expected ordered packing arrangements.     

Drying dissipative patterns of colloidal crystals of silica spheres on a cover glass at the regulated temperature and humidity

Influences of temperature and humidity on the drying dissipative patterns of colloidal crystals of silica spheres (103 nm in diameter) were studied. The broad ring pattern, which is one of the typical macroscopic drying structures, became sharp as temperature rose and/or humidity decreased. Furthermore, number of the spoke-like cracks decreased as temperature and/or humidity increased. The water evaporation from a liquid surface to air and the convectional flow of water and colloidal spheres were important for the macroscopic pattern formation.     

The migration of styrene butadiene latex during the drying of coating suspensions: when and how does migration of colloidal particles occur?

Surface elemental compositions of model latex clay coatings on an impervious substrate consolidated under various conditions were measured using the XPS technique, in order to clarify when and how colloidal latex particles migrate to the surface during drying. Under similar drying conditions, surface carbon content decreased with the addition of a water-soluble polymer to the coating colors, while remaining virtually unchanged for coatings of different coat weights made with a given color, indicating that surface carbon content variation is mainly caused by migration of latex rather than of water-soluble polymer. The results also showed that for coatings made with a given suspension, surface carbon content decreased with increasing delay time between coating and heating. For coatings frozen during consolidation and dried by sublimation, surface carbon content increased with increasing drying time before freezing. These results suggest that for the model coatings studied, latex migration mainly occurs after coating application before capillary formation during the initial drying stage when coatings are in the liquid phase, contradicting both the conventional capillary transport and boundary wall migration mechanisms. An alternative mechanism which attributes latex migration to surface trapping effect and to higher Brownian mobility of the smaller latex particles compared with pigment appears to provide a systematically consistent explanation to those phenomena. The new particle migration mechanism implies that segregation of colloidal particles is a ubiquitous phenomenon that would occur not only during the drying of paper coatings but also during consolidation of colloidal films containing particles of different sizes. This is of great importance in the control of surface compositions of nanocomposite coatings.     

Salt-induced protein phase transitions in drying drops

Protein phase transitions in drying sessile drops of protein-salt-water colloidal systems were studied by means of optical and atom-force microscopy. The following sequence of events was observed during drop drying: attachment of a drop to a glass support; redistribution of colloidal phase due to hydrodynamic centrifugal stream; protein ring formation around the edge; formation of protein spatial structures inside a protein ring that pass into gel in the middle of the drop; salt crystallization in the shrinking gel. It was assumed that rapid drying of a protein ring over the circle of high colloidal volume fraction and low strength of interparticle attraction leads to formation of colloidal glass, whereas gel forms only in the middle of the drop at very low protein volume fraction and strong attraction between the particles. Before gelation, colloidal particles form fractal clusters. In dried drops of salt-free protein solutions, no visual protein structures were observed. Structural evolution of protein in sessile drying drops of protein-salt aqueous colloidal solutions is discussed on the basis of experimental data.     

Harnessing Colloidal Crack Formation by Flow‐Enabled Self‐Assembly

Self‐assembly of nanomaterials to yield a wide diversity of high‐order structures, materials, and devices promises new opportunities for various technological applications. Herein, we report that crack formation can be effectively harnessed by elaborately restricting the drying of colloidal suspension using a flow‐enabled self‐assembly (FESA) strategy to yield large‐area periodic cracks (i.e., microchannels) with tunable spacing. These uniform microchannels can be utilized as a template to guide the assembly of Au nanoparticles, forming intriguing nanoparticle threads. This strategy is simple and convenient. As such, it opens the possibility for large‐scale manufacturing of crack‐based or crack‐derived assemblies and materials for use in optics, electronics, optoelectronics, photonics, magnetic device, nanotechnology, and biotechnology.     

Generalized Hertzian model for the deformation and cracking of colloidal packings saturated with liquid

The process of drying colloidal dispersions generally produces particulate solids under stress as a result of capillary or interparticle forces. The derivation of a constitutive relation on the basis of Hertzian contact mechanics between spheres provides a model for quantitatively predicting the conditions under which close-packed colloidal layers form continuous void-free films or homogeneous porous films or crack under tensile stresses.     

Centimeter-scale colloidal crystal belts via robust self-assembly strategy

Centimeter-scale poly(acrylic acid-co-DVB80) (PAA) 3D colloidal crystal belts were prepared via a novel robust vertical deposition technique based on negative pressure and curvature substrate of the glass vial. The formation of PAA colloidal crystal belts was investigated. The results indicated that curvature could control the dimension of PAA colloidal crystal belts. Well-controlled negative pressure resulted in rapid fabrication of well-defined PAA colloidal crystal belts. Curvature substrate of glass vial could distribute shrinking stress in the process of drying of colloidal films. Strong hydrogen bonding interactions among carboxyl groups on the surface of PAA colloidal particles was responsible for PAA colloidal crystal belts with closed-packing characteristics.