Toughening by Monoclinic Zirconia

The toughening induced by monoclinic ZrO₂ in the absence of microcracking was investigated, using ZnO as the host material. Toughness levels K_c in excess of the host toughness K_c^M were achieved, attaining a peak toughness K_c/K_c^M ∼1.7, at monoclinic ZrO₂ volume concentrations 0.2. This toughening is attributed to crack/particle interactions, associated with the deflection and bowing of the crack by the residual strain field around the monoclinic ZrO₂ particles.     

Catalyzing the curing reaction of a new benzoxazine-based phenolic resin

The effect of potential catalysts on the curing reaction of a new type of phenolic resins obtained from benzoxazine precursors is studied. These novel resins solve the shortcomings of traditional phenolics because they cure by a ring-opening mechanism that avoids the release of volatiles. Isothermal and nonisothermal differential scanning calorimetry (DSC) data is used to determine the influence of the catalysts on the curing kinetics. Fourier transform infrared (FTIR) spectroscopy is also applied. The benzoxazine chosen for this study is a purified benzoxazine monomer based on bisphenol-A, formaldehyde, and aniline. The as-synthesized benzoxazine precursor is also studied to determine the influence of the dimers and higher oligomers in the curing mechanism. The presence of these structures seems to catalyze the curing reactions. The activation energy and overall reaction order of the as-synthesized precursor are determined. Among the catalysts tested, adipic acid shows the most promising results. For all the cases studied the curing reaction is autocatalyzed up to a diffusion-controlled stage. © 1995 John Wiley & Sons, Inc.     

NMR and sedimentation studies of a polymeric steric stabilizer for alumina

The sedimentation behavior of alumina powder has been studied in the presence of poly-vinylpyrrolidone (PVP) and poly(vinylpyrrolidone-co-vinyl acetate) (PVP/VA) in both thermodynamically “good” and “poor” solvents for the PVP homopolymer. PVP/VA provides higher sediment densities than does its PVP homopolymer counterpart. Solutionstate ¹³C-T₁ spin-lattice relaxation measurements were made on analogous mixtures both with and without alumina powder. The NMR results suggest that the PVP/VA copolymer is anchored to the alumina powder surface by means of VA moieties, whereas the PVP moieties extend into the continuous phase of the slurry medium. Thus, the higher settling densities that are observed in the presence of PVP/VA can be attributed to a steric stabilization mechanism. © 1993 John Wiley & Sons, Inc.     

Reciprocating flow ion exchange part II: Application to saline water softening

The “hardness” components in sea water can be considerably reduced by means of a new economical fixed bed technique called “Reciprocating Flow Ion Exchange”, when used in conjunction with a closed cycle exchanger-evaporator system. Removal of 87.9% of the calcium and 54.5% of the magnesium in sea water has been obtained with an overall flow rate of 5.0 U. S. g. p. m./sq. ft. Results from bench scale and a 5,000 g. p. d. pilot plant were identical. The virtually continuous cyclic steady-state process requires a small amount of exchanger (0.5 to 2% of the usual ion exchange methods, such as conventional fixed beds or fluidized beds). The effects of variation in operating parameters are discussed.     

Preparation of a microporous composite: Encapsulation of paper by polyethylene

A rapid polymerization method for in situ synthesis of polyethylene in a typical paper matrix of cellulose fibers is described. The unique properties of this double matrix, polyethylene in cellulose, are the result of performing the polymerization in a nonsolvent such that simultaneous polymerization and crystallization takes place yielding a nascent morphology. The morphology has been studied by scanning electron microscopy and was found to be different from what is usually obtained for melt crystallized polyolefins. Optical microscopy shows the polyethylene to be present as a complementary matrix with respect to the basic fiber construct. Mechanical, optical, and other properties of encapsulated filter paper have been measured using standard TAPPI tests. The results show a general improvement in physical properties for a range of “add ons” from 0 to 27%. Wet-strength and opacity undergo major changes.     

Über die Bildung des Kakaoaromas aus seinen Vorstufen

Formation of Cocoa Aroma from Its Precursors Isolation and chemical composition of a highly purified mixture of aroma-precursors from raw cocoa were extensively studied and the alterations due to heating at roasting temperatures were followed quantitatively. Cocoa aroma is formed in the course of a Maillard reaction between amino acids and reducing sugars. Participation of oligopeptides in the alterations that are specific for the process of roasting could be detected for the first time. From the high-boiling components present in the reaction product, a fraction having the typical cocoa flavour could be isolated and resolved by gas chromatography. The consequences of these observations on the technology of roasting of cocoa are discussed.     

Factors influencing the efficacy of an interfacial modifier for the interface in an immiscible polymer blend

The modification of the interface in immiscible polymer blends is critical in order to optimize physical properties. Despite the great commercial importance of polymer blends, many aspects of the emulsification process remain unclear In this paper, it will be shown that an emulsification curve can be used to estimate the influence of the architecture molar mass of styrene/hydrogenated butadiene block copolymer interfacial modifiers on the emulsifion of polystyrene/ethylene-propylene rubber blends under melt processing conditions. An expression for eing the critical amount of copolymer to saturate the interface, as well as aspects concerning the localisation of the modifier in the blend system will also be addressed.     

A thermomechanical investigation of highly cold-drawn polycarbonate

A new technique detecting molecular motions in drawn polymers was applied to highly cold-drawn polycarbonate of bisphenol A. It is shown that the sample exhibits thermal shrinkage in three steps with the temperature increase up to above the glass transition temperature. The molecular relaxation at the highest temperature is due to the glass transition. The other two molecular motions at the lower temperature are those of main chain in the glassy state and they correspond to the molecular motions as revealed in dielectric measurement by Sacher.¹ By using the general theory of the thermal analysis by Ozawa,² the apparent activation energies of these molecular motions were obtained: for the highest temperature 110 kcal/mole, and for the lowest temperature, 33.5 kcal/mole. The impact strength and the cold workability of this polymer are also discussed in relation to these molecular motions.