Poly(Styrene‐Divinylbenzene) Based Media for Liquid Chromatography

The latest developments and in particular important synthetic aspects for the preparation of modern poly(styrene‐divinylbenzene) (PS‐DVB) based liquid chromatography (LC) supports are reviewed. In this context, the chemistry of particular porous and nonporous, functionalized, monolithic, coated silica and more specialized mixed organic PS‐DVB media is covered. Special consideration is given to modern approaches such as micro‐(μ)‐HPLC and coating techniques and their most important applications. Synthetic particularities relevant to the corresponding applications are outlined.     

Steric requirements for coal swelling by amine bases

A set of six coals ranging in rank from lignite to hvA bituminous was swollen with a series of alkyl-substituted pyridines and a smaller set of 4-alkylanilines. The size and branching of the alkyl groups was varied and the effect of this variation on the dissolution of the amines in the coal and the resulting coal swelling was measured volumetrically. In a few cases, substituents which hindered the amine nitrogen were studied. The lignite and subbituminous coal have a much higher tolerance to branched, bulky groups than do the bituminous coals. The presence of tertiary groups in a solute strongly inhibits their dissolution in bituminous coals. Bituminous coals behave as if extensive parallel packing of structures occurs. Often, they can accept very large planar groups but have a low capacity for branched groups.     

The Effect of Moisture Content in Epoxy Film Adhesives on their Performance. II. T-Peel and 105°C Lap Shear Strength

The benefits of adhesively bonded structures are well known. However, the most significant factor limiting the extensive application of metal bonding in primary aerospace structures is the prevailing lack of confidence in its long term durability under hostile environmental conditions.^1,2     

The growth of ambient aerosols in the conditions of the respiratory system

The effect on ambient aerosols of exposure to the conditions of the respiratory system was determined by sampling simultaneously through two dichotomous samplers in parallel. In one of the samplers the aerosol was brought to 37°C and near 100% relative humidity before passing through the virtual impactor. The results show that, as a result of humidification, about 10–15% by mass of the aerosol which would normally been collected in the fine (less than 2.5 μm aerodynamic diameter) fraction of the sample grows sufficiently when humidified to be collected with the coarse fraction. It is suggested that the direct application to inhalation studies of dichotomous sampler results should be approached with some caution.     

Graft copolymerization onto rubber. VII. Graft copolymerization of methyl methacrylate onto rubber using potassium peroxydisulfate catalyzed by silver ion

The graft copolymerization of methyl methacrylate onto natural rubber (NR) was carried out varying the concentration of monomer, initiator, thiourea, and silver nitrate over a wide range. The grafting reaction was temperature-dependent. From the Arrhenius plot, the overall energy of activation was computed. A suitable reaction scheme and rate expression for the rate of polymerization was suggested.     

Fractoemission from Lead Zirconate-Titanate

We present measurements of the electron, positive ion, and photon emission accompanying the fracture in vacuum of poly-crystalline 95/5 lead zirconate-titanate. The intensities of the charged-particle components of this fractoemission are shown to depend strongly on the direction (relative to the direction of fracture) and magnitude of polarization. The most intense emission is observed when the fracture surfaces are perpendicular to the polarization direction. The emission intensity increases monotonically with polarization. These results are interpreted in terms of a model involving charge separation on the fracture surfaces leading to a microdischarge during fracture. Implications to the interpretation of triboluminesence effects are discussed.     

Stress in Leached Phase-Separated Glass

When a phase-separated glass is leached, stresses develop because of release of thermal stresses, creation of surface area, ion exchange, and hydration. Analyses are presented for the thermal stresses, including the portion that develops on cooling from the heat-treatment temperature to the setting temperature of the less viscous phase. During leaching, the interfacial energy of the residual phase increases, so that phase tends to contract. A more important effect is the contraction caused by removal of alkali and B₂O₃ from the residual phase during leaching. The extent of removal of B₂O₂ decreases with heat-treatment time, t_H , because the scale of the microstructure increases as t^1/3_H. The change in residual B₂O₂ content with t_H is shown to be consistent with diffusion-controlled ion exchange. The dependence of stress on t_H in partially leached glasses, measured by Drexhage and Gupta, results principally from the change in extent of ion exchange; the reduction in surface area with increasing t_H also has a significant effect on the stresses.