Investigations of a series of PPDI-based polyurethane block copolymers. II. Annealing effects

In a previous study, the morphologies of a group of paraphenylene diisocyanate (PPDI)-based polyurethane block copolymers were examined. These polyurethanes exhibited a multiphase structure with an interfacial boundary thickness estimated to be on the order of 1 nm and crystallization of the polyoxytetramethylene (POTM) flexible segment. Further studies involving annealing of these polyurethanes are reported here. An annealing time of 4 h was used, and the annealing temperature varied from 125 to 200°C. The samples have been characterized using differential scanning calorimetry (DSC) and with wide- and small-angle x-ray scattering (WAXS, SAXS) in order to determine the effects of annealing on the microphase structure. Annealing increases the phase separation of the two phases as evidenced by sharper endotherms in DSC thermograms and increased intensities in WAXS diffractometer traces. Annealing also slightly increases the transition zone thickness and long-period spacing. At the highest annealing temperature in this study, the long-period spacing increases dramatically due to hard segment domain aggregation.     

13C and 15N NMR spectra of 4-substituted-1-dimethylphosphonopiperazines

¹³C and ¹⁵N NMR chemical shifts and ¹³C-³¹P and ¹⁵N-³¹P coupling contants are reported for a series of ten 4-substituted-1-dimethylphosphonopiperazines.     

The four-jet structure of large transverse momentum events inpp interactions at the ISR

Deep inelastic proton-proton collisions have been recorded with the Split-Field-Magnet Detector (SFM) at the CERN Intersecting Storage Rings (ISR) by triggering on a single particle at high transverse momentum. Full reconstruction of the charged particles in these collisions was performed. In this paper we demonstrate the existence of a structure comprised of four jet-like clusters, two longitudinal and two transverse with respect to the beam, as would be expected from hard scattering of proton constituents.     

Early identification of isovaleric aciduria using photodiode array detection for liquid chromatographic profiling of urinary carboxylic acids

The 190 nm high performance liquid chromatographic photodiode array profiling of the urinary carboxylic acids of the first urine of a newborn affected with isovaleric aciduria afforded an abnormal peak at 27.8 min. This peak was greatly increased in the carboxylic acid profiling of the 14 h urine sample from the same infant. Isolation of this peak by fraction collecting; solvent extraction of the eluent; trimethylsilyl derivatization of the residue and gas chromatographic/mass spectrometric analysis identified the compound as isovalerylglycine. Correlation of the 190 nm absorbance of isovalerylglycine (y) with concentration (x) afforded a least squares curve: y = 476.4x-13.72 (r = 0.99); run-to-run variation 6.92%; day-to-day variation 8.88% with a minimum detectable concentration of 25 micrograms/ml.