Theory of “Cohesive” vs “Adhesive” Separation in an Adhering System

It is shown that there is limited validitity to the doctrine that true interfacial separation, in an adhering system, is highly improbable. An analysis employing the Griffith-Irwin crack theory yields these results: The important parameters are, difference in elastic moduli, ΔE; differences in g, the energy dissipation per unit crack extension; thickness, Δ₁ or δ₂, of the region where dissipation occurs; and the presence or absence of strong interfacial bonds. If the forces across the interface are appreciably weaker than the cohesive forces in either phase, there is a strong minimum in g at the interface. For flaws of equal size, an interfacial flaw will be the site of initiation of failure. If strong interfacial bonds are present, then if Δg and ΔE have the same sign, failure is most probable, deep within one phase. If Δg and ΔE have opposite signs, failure may be initiated, and may propagate, at a distance δ from the interface, in the phase with lower g. This may be mistaken for weak-boundary layer failure.     

Inhibitor properties of “green” pigments for paints

Zinc chromate is one of the anticorrosive pigments most frequently used in the formulation of primers. However, its environmental aggressiveness and toxicity severely restrict its use, and different green alternatives have been proposed in order to replace zinc chromate. In the last decade, the behaviour of zinc phosphate as anticorrosive pigment has been intensively researched. During this time, various modifications have been made to this family of pigments to improve its properties, and a “second generation” of phosphate pigments, incorporating elements such as molybdenum, aluminium, or iron, has been produced. In this paper, the inhibitive properties of zinc phosphate and three second-generation phosphates have been investigated, using zinc chromate pigment as a reference. Pigment extract solutions, at different values of pH, have been used as corrosive media. Carbon steel samples were immersed in such solutions and their corrosion rates were measured using electrochemical techniques. The data obtained suggest that zinc chromate provides the highest percentage of inhibition in neutral and basic solutions, but phosphate-based pigments showed better results in acid solutions. Given this performance advantage, together with their less harmful environmental impact, these phosphate-based pigments can be proposed as realistic alternatives to chromates in the formulation of protective paints for use in acidic conditions.     

Comment on “Optimization of a spectrally tunable LED daylight simulator”

This is a comment on “Optimization of a spectrally tunable LED daylight simulator” (Color Res Appl. 2017;42:419‐423). We found that full widths at half maximums (FWHMs) of light‐emitting diodes (LEDs) used in the six channels for daylight simulators given by Wei were 50 nm, not 30 nm. Therefore, it is impossible to implement AA‐grade daylight simulators with six LED channels. By our simulation, it was found that at least seven LEDs channels with FWHMs of 30 nm are required to produce a spectrally tunable daylight simulator with AA‐grade by appropriate intensity combinations. Furthermore, the spectrally tunable AA‐grade daylight simulators using six, five, and four channels were simulated. We have first reported that the scheme for the spectrally tunable daylight simulator with AA‐grade using three, four, and five types of phosphors or quantum dots excited by an ultraviolet LED.     

Toward “Rubbery” nanoparticles

The synthesis of electrically Conducting Natural Rubber (CNR) nanoparticles from natural rubber (cis 1, 4 polyisoprene) by a simple chemical doping technique is reported for the first time. Much before the establishment of conjugation as a precondition for polymers to be conducting a typical nonconjugated polymer like cis 1,4 polyisoprene was shown to develop intrinsic conductivity on doping. However, the possibility of developing conducting nanoparticles of natural rubber by doping has never been explored. Doping of natural rubber solution with Antimony pentchloride is found to lead to the formation of nanosized rubber particles with improved thermal stability and lower degradation characteristics than that of pristine rubber. Transmission electron microscopy and Dynamic Light Scattering experiments revealed a highly uniform dispersion of the particles with sizes in the range of 4 nm. The doped nanoparticles are found to retain “rubbery” properties of natural rubber and therefore these can be rightly termed as Rubber Nano particles. The development of nanoparticles of rubber assumes great significance in that it would lead to hitherto unknown applications for natural rubber in micro applications‐like sensors, and optoelectronics devices to macro applications such as compatible reinforcing fillers for elastomers and plastics to replace conventional fillers like carbon particles. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

“HETEROGENIZING” HOMOGENEOUS CATALYSTS

For many years, it has been customary to classify catalysts as “homogeneous” or “heterogeneous.” The former commonly operate through the formation of “intermediate compounds,” and the latter, by adsorption of the reactants on the catalyst surface. The line between the two is a fine one, for the distinction between adsorption and compound formation is not at all clear, and seems to be becoming less and less clear as we learn more about adsorption. In recent years, several writers [l-7] have stressed the point that there is a good deal of overlap between homogeneous and heterogeneous catalysis. Experimental evidence supporting this point of view is accumulating, and while we are not prepared to say that there is no distinction, we can say with certainty that many homogeneous catalysts can be converted into heterogeneous ones, retaining the advantages of great activity and selectivity inherent in homogeneity and, at the same time, assuming the ready recovery which is the great advantage of heterogenity. In practice, of course, the matter is not quite that simple, for other factors must be considered. On the whole, however, many advantages have been found in the use of heterogenized homogeneous catalysts.     

Photoinduced controlled/“living” polymerization of methyl methacrylate with flavone as photoinitiator

Photochemically mediated controlled/“living” polymerization of methyl methacrylate (MMA) triggered by flavone was studied. The polymerization was performed in ethanol at ambient temperature with CuBr₂/Tris(2‐dimethylaminoethyl)amine (Me₆TREN) as complex catalyst and ethyl 2‐bromoisobutyrate (EBiB) as initiator. The molar mass of poly(methyl methacrylate) (PMMA) was obtained and exhibited relatively narrow molecular weight distribution (M_w/M_n) which was characterized by gel permeation chromatography (GPC). Chain extension further indicated that the living nature was maintained in the photopolymerization system. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43845.