INVITED REVIEW STABILITY OF COLLOIDAL DISPERSIONS

The stability of colloidal dispersions has traditionally attracted considerable attention in the chemical literature because of its origins in the physical chemistry of electrostatic and steric interactions between surfaces immersed in liquids. Moreover, progress in the physics and chemistry of stability phenomena has a direct impact on chemical engineering research, since stability of dispersions plays an important role in the rheology and transport properties of charged particles in liquids, separation processes (such as membrane filtration and solid/liquid separation), deposition and particulale fouling phenomena and numerous other processing operations. This paper presents a discussion of physical and chemical factors that affect colloidal stability and, in addition, presents an overview of the status of current research needs in this area. In addition to electrostatic and steric effects, some recent studies on the role of bulk motion of the supporting liquid on stability are also discussed. The emphasis throughout is on the stability of dilute dispersions, in which simultaneous interactions between more than two particles are negligible. Some major research needs in the above areas are also identified.     

Normally Oriented Adhesion versus Friction Forces in Bacterial Adhesion to Polymer‐Brush Functionalized Surfaces Under Fluid Flow

Bacterial adhesion is problematic in many diverse applications. Coatings of hydrophilic polymer chains in a brush configuration reduce bacterial adhesion by orders of magnitude, but not to zero. Here, the mechanism by which polymer‐brush functionalized surfaces reduce bacterial adhesion from a flowing carrier fluid by relating bacterial adhesion with normally oriented adhesion and friction forces on polymer (PEG)‐brush coatings of different softness is studied. Softer brush coatings deform more than rigid ones, which yields extensive bond‐maturation and strong, normally oriented adhesion forces, accompanied by irreversible adhesion of bacteria. On rigid brushes, normally oriented adhesion forces remain small, allowing desorption and accordingly lower numbers of adhering bacteria result. Friction forces, generated by fluid flow and normally oriented adhesion forces, are required to oppose fluid shear forces and cause immobile adhesion. Summarizing, inclusion of friction forces and substratum softness provides a more complete mechanism of bacterial adhesion from flowing carrier fluids than available hitherto.     

Off-line modelling and planning of optimal clamping forces for an intelligent fixturing system

An intelligent fixturing system (IFS) for machining aims to adaptively adjust the clamping forces to achieve minimum deformation of the workpiece according to the cutter position and the cutting forces. This paper presents the concept, architecture, control scheme, models and methodologies for an IFS. Using off-line simulations and on-line experimental verifications, the performance of the proposed IFS is evaluated and verified. As adaptive clamping forces appropriate to the dynamic machining environment are employed, the IFS offers higher quality of machined parts and greater robustness to disturbances. This system is suitable for application in high-precision machining environment as well as flexible manufacturing systems (FMS).     

Chemical Interactions and Their Role in the Microphase Separation of Block Copolymer Thin Films

The thermodynamics of self-assembling systems are discussed in terms of the chemical interactions and the intermolecular forces between species. It is clear that there are both theoretical and practical limitations on the dimensions and the structural regularity of these systems. These considerations are made with reference to the microphase separation that occurs in block copolymer (BCP) systems. BCP systems self-assemble via a thermodynamic driven process where chemical dis-affinity between the blocks driving them part is balanced by a restorative force deriving from the chemical bond between the blocks. These systems are attracting much interest because of their possible role in nanoelectronic fabrication. This form of self-assembly can obtain highly regular nanopatterns in certain circumstances where the orientation and alignment of chemically distinct blocks can be guided through molecular interactions between the polymer and the surrounding interfaces. However, for this to be possible, great care must be taken to properly engineer the interactions between the surfaces and the polymer blocks. The optimum methods of structure directing are chemical pre-patterning (defining regions on the substrate of different chemistry) and graphoepitaxy (topographical alignment) but both centre on generating alignment through favourable chemical interactions. As in all self-assembling systems, the problems of defect formation must be considered and the origin of defects in these systems is explored. It is argued that in these nanostructures equilibrium defects are relatively few and largely originate from kinetic effects arising during film growth. Many defects also arise from the confinement of the systems when they are ‘directed’ by topography. The potential applications of these materials in electronics are discussed.     

The Importance of Bonded Structural Material

Gluing is of tremendous importance to the wood industry. About 70% of all wood used today involves gluing. As an increasing amount of lower quality wood is used in the future, gluing will become even more important. Additional developments in harvesting previously unused species and forest residues and cleaning dirty material, and a means to reclaim urban waste wood, are needed to assure an adequate wood supply. New or improved economical adhesive systems will be important in accelerating the development of glued products. The future of the wood products industry lies with the use of glue, since the wood raw material will continue to be harvested in ever smaller sizes.     

Effects of bulk and surface properties of materials on adhesion-induced deformations between submicrometer diameter particles and substrates

—Spherical particles of polyvinylidene fluoride (PVF₂), of 0.3 μm diameter, were deposited onto various substrates including polyester, a polyester-polydimethylsiloxane block copolymer (hereafter referred to as PSBC), and polished silicon. The adhesion force-induced deformations between the particles and substrates were then observed using scanning electron microscopy (SEM). It was found that the particles embedded most deeply into the soft PSBC. No embedding of the particles into the Si wafers was observed, although the particles, themselves, appeared to flatten. The particles were also observed to embed into the polyester, although to a lesser extent than they did into the PSBC. Moreover, when the particles contacted samples of polyester which had been plasma-treated in argon, the embedding decreased. Measured contact area diameters are compared to predictions of various models of adhesion. The effect of the thickness of a conducting (Au/Pd) coating on the appearance of the contact zone is also discussed.     

The role of scale resolution versus inter-particle cohesive forces in two-fluid modeling of bubbling fluidization of Geldart A particles

Coarse grid simulations of Geldart A particles in bubbling fluidized beds using standard two-fluid (TF) models, where the constitutive laws are based on the homogeneity of sub-grid scale structures, have been demonstrated to be unsuccessful due to the existence of significant sub-grid scale heterogeneous structures. However, a definite consensus on the fundamental origin of the failure is still lacking. Some claim that the existence of significant inter-particle cohesive forces results in the sub-grid scale heterogeneous structures which takes the form of agglomerates or clusters; others claim that the inter-particle cohesive forces are not the dominant factor, and that the poor performance of TF models is primarily due to the fact that the grid sizes and the time step used in previous studies are too coarse to fully resolve the bubbling structure. To this end, a short overview is firstly presented to discuss the role of scale resolution and inter-particle cohesive force in two-fluid modeling of Geldart A particles; We then qualitatively explain, using a state-of-the-art discrete particle method, why the methods based on the existence of aggregates or clusters work quite well, although the sub-grid scale structure is not properly identified, that is, the sub-grid scale structure takes the form of a bubble-emulsion phase.     

Limit of accuracy in laser fabrication with metal powder

The research presented in this paper focuses on the laser-powder interaction. Through the experiment with metal powder in micrometers, we found that, in an invariable laser power density, the thickness of the final fabricated thin wall was similar to the geometrical dimension of the powder line, but could be much greater than the laser focus spot, even greater than two orders of magnitude. Furthermore, this paper showed that, the unmelted and semi-fused particles were concentrated. Thus,in this paper, combining the optical scattering theory with capillarity and infiltration theory pointed out the inducement effect of laser and the self-melting of powder. Based on the experimental phenomena and theory, we get our own ideas on the laser micro-fabrication.     

The Chemistry of PCR Primers: Concept and Application

DNA is a typical organic compound with marked differences from other chemicals and biopolymers because DNA can be amplified by the enzyme polymerase. DNA can be, in principle, amplified from a single copy by the polymerase chain reaction (PCR). In this review, we focus our attention on the chemistry of PCR primers. Because PCR is basic technology in biology research fields, we sometimes use chemically labeled primers without any awareness of the chemistry they leave behind. We would like to emphasize that chemically labeled primers contain a lot of potential for different chemistry ideas and much study is still necessary to advance PCR for single-nucleotide polymorphism (SNP) typing, genetic diagnosis, and other fields. Two categories of primers, affinity-capture primers and signaling primers, are discussed from the viewpoints of their chemical concepts and applications. Affinity-capture primers are used for purification, isolation, and manipulation of PCR products by high specificity and affinity to the cognate molecules by molecule molecule interactions, whereas signaling primers report the hybridization and/or progress of PCR amplification by a signal change, in most cases by a fluorescence change. The content of this review may be useful for a better understanding of the chemistry of PCR primers and, more importantly, for the invention of novel PCR chemistry.