Glass transitions in hydrogen-bonded polymer complexes

Mutual precipitates of poly (N, N-dimethyl acrylamide) and poly (4-hydroxystyrene) were collected from dioxane, methanol, or acetone. The glass transition (T_g) temperatures of the precipitates are higher than the weight-average values. Clear films cast from dimethylformamide solutions have lower T_g values. Complexation also occurred between poly (ethyl oxazoline) and poly (4-hydroxystyrene) in dioxane and between poly (vinyl pyrrolidone) and poly (4-hydroxystyrene) in methanol. Again, the glass transition temperatures of the precipitates are higher than the values for the blend films. The ΔC_p values associated with the glass transitions of the complexes are smaller than those of the blends having the same compositions. Negative excess heat capacities of mixing have been observed for several precipitates.     

Specific high performance liquid chromatographic determination of the molecular weight and concentration of hyaluronic acid in complex mixtures by labelled hyaluronate binding proteins.

A simple High performance liquid chromatographic (HPLC) method for the specific determination of the molecular weight and concentration of hyaluronic acid (HA) in complex mixtures has been developed. Hyaluronate-binding proteins isolated from bovine cartilage labelled by 125I or fluoresceinisothiocyanate were used as specific markers. The specific binding affinities of the markers were compared and were found to have association constants of 1.6 x 10(7) M-1 and 1.2 x 10(7) M-1 respectively. The HA levels and molecular weight distributions can be easily determined in the range 10-500 ng/mL in complex mixtures by the use of markers, molecular sieving HPLC columns and appropriate detectors. It has been demonstrated clearly that the method is useful for the highly specific determination of the parameters in complex biological samples such as serum and synovial fluids and is recommended for clinical applications.     

Three-phase model of a chiral quark bag

A three-phase model of a hybrid chiral quark bag is proposed. In addition to the phases of asymptotically free current quarks and of totally colorless mesons, the model contains the intermediate phase of massive constituent quarks. A self-consistent solution with an account for the “Dirac sea” contribution is found in the (1+1)-dimensional case. The dependence of the bag parameters on the parameters of the theory is investigated analytically and numerically. Translated from Teoreticheskaya i Matematicheskaya Fizika, Vol. 117, No. 2, pp. 263–299, November, 1998.     

Laser induced air breakdown using 0.355, 0.532, and 1.06 µm radiation

Studies of breakdown threshold intensity for air at various pressures in the range of 24–760 torr using 0.355, 0.532 and 1.06 μm radiation are reported. We observep ^−0.8 scaling ofI _th at 1.06 μm and a weak scaling ofp ^−0.4 at 0.532 and 0.355 μm radiation. Strong dependence of breakdown spot size on laser power but weak dependence on air pressure is observed.     

New olefinic functionalized disilanes. Synthesis and NMR spectroscopical investigations

The new olefinic substituted aminodisilanes, which are obtained from the reaction of organometallic reagents with aminochlorodisilanes, are converted into the chlorodisilanes by equilibration reactions or treatment with HCI. The resulting olefinic functionalized disilanes are identified by means of ²⁹Si, ¹³C, ¹H NMR and GC MS measurements.     

Structure of the crystal solvate of the dipyridinium salt of 2,2′-bis[1,3-bis(dicyanomethylene)indane] with acetonitrile

L. Ya. Karpov Physical Chemical Research Institute. Translated from Zhurnal Strukturnoi Khimii, Vol. 32, No. 3, pp. 141–144, May–June, 1991.     

Liquid chromatographic-mass spectrometric studies on rifamycin antibiotics

The use of a direct liquid introduction type liquid chromatographic-mass spectrometric interface to study highly thermally labile rifamycin antibiotics is described. Using negative ionization, abundant molecular ions were observed, and the spectra, also contained structurally significant fragments. Variation of the high-performance liquid chromatographic parameters did not change the spectra, thus making it easy to change chromatographic conditions. In quantitative studies, a surprising correlation was found, indicating that the mass spectrometric signal was proportional to the square of the sample concentration.