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.     

Semi-1 thermoplastic interpenetrating polymer networks of physically crosslinked poly(n-butyl acrylate) and polystyrene

Poly(n-butyl acrylate) (PnBA) chemically crosslinked with tetraethylene glycol dimethacrylate (TEGDM) and physically crosslinked PnBAs produced by neutralization of poly(n-butyl acrylate-stat-acrylic acid) with NaOH or Ca(OH)₂ were prepared as a polymer I network. Each polymer I was swollen with styrene and cured in situ into semi-IPN-TEGDM, semi-IPN-Na, or semi-IPN-Ca, respectively. Both physically crosslinked polymers maintained their shapes during the swelling procedure. Dynamic mechanical spectroscopy indicated that good mixing of the two polymers took place in the semi-IPN-Ca as well as in semi-IPN-TEGDM, but a distinct phase separation occurred in the semi-IPN-Na. These results were supported by their transparent or optical opaque appearances, respectively. Annealing at 180°C developed further phase separation in the semi-IPN-Na, but very little in the semi-IPN-Ca. Analyses by the incompatibility number (based on the modulus–temperature curve) and the calculation of individual phase compositions (from the glass transition temperature shifts) were used in estimating the extent of molecular mixing.     

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.     

Oberflächenlipide und Lipidpolymere von Pflanzen

Surface Lipids and Lipid Polymers of Plants The protective skin of higher plants, or cuticle, consists of a lipid coating and the characteristic polymer lipids cutin and suberin. The lipid coating contains hydrocarbons, wax, triterpenes, sterols and sometimes aldehydes and ketones. Cutin, an estolid, unsoluble in water and organic solvents, is built up by hydroxylated fatty acids with 16 and 18 C-Atoms. Suberin is in its constitution very similar to cutin. Its characteristic compounds are hydroxylated dicarbonic acids. To the degradation of cutin and suberin by men and animals some references have been given.